{"id":36566,"date":"2026-08-31T12:13:11","date_gmt":"2026-08-31T06:43:11","guid":{"rendered":"https:\/\/www.legalraasta.com\/blog\/?p=36566"},"modified":"2026-08-31T12:13:11","modified_gmt":"2026-08-31T06:43:11","slug":"cdsco-registration-for-disposable-medical-devices","status":"publish","type":"post","link":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/","title":{"rendered":"CDSCO Registration for Disposable Medical Devices in India: Eligibility, Process, Documents, Fees &amp; Compliance"},"content":{"rendered":"<p><img fetchpriority=\"high\" decoding=\"async\" class=\"alignnone wp-image-36567 size-fusion-1200\" src=\"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-1200x633.jpg\" alt=\"CDSCO Registration for Disposable Medical Devices\" width=\"1200\" height=\"633\" srcset=\"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-200x105.jpg 200w, https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-300x158.jpg 300w, https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-400x211.jpg 400w, https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-600x316.jpg 600w, https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-768x405.jpg 768w, https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-800x422.jpg 800w, https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-1024x540.jpg 1024w, https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices-1200x633.jpg 1200w, https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg 1280w\" sizes=\"(max-width: 1200px) 100vw, 1200px\" \/><\/p>\n<p><span style=\"font-weight: 400\">Selling syringes, gloves, or IV sets in India without a licence sounds harmless. It isn&#8217;t. CDSCO Registration for Disposable Medical Devices is a legal requirement, not paperwork you can skip and fix later.<\/span><\/p>\n<p><span style=\"font-weight: 400\">Miss it, and customs holds your shipment or a state drug inspector shuts your unit down mid-production. Get it right the first time, and you&#8217;re selling to hospitals, government tenders, and export markets without a compliance headache hanging over you.<\/span><\/p>\n<p><span style=\"font-weight: 400\">This guide walks through classification, the actual <\/span><a href=\"https:\/\/www.legalraasta.com\/cdsco-registration\/\"><span style=\"font-weight: 400\">CDSCO filing<\/span><\/a><span style=\"font-weight: 400\"> steps, fees as they stand in 2026, and the mistakes that get applications rejected. Talk to LegalRaasta&#8217;s regulatory team if you&#8217;d rather have someone file this correctly the first time.<\/span><\/p>\n<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_73 counter-hierarchy ez-toc-counter ez-toc-grey ez-toc-container-direction\">\n<div class=\"ez-toc-title-container\">\n<p class=\"ez-toc-title\" style=\"cursor:inherit\">Contents<\/p>\n<span class=\"ez-toc-title-toggle\"><a href=\"#\" class=\"ez-toc-pull-right ez-toc-btn ez-toc-btn-xs ez-toc-btn-default ez-toc-toggle\" aria-label=\"Toggle Table of Content\"><span class=\"ez-toc-js-icon-con\"><span class=\"\"><span class=\"eztoc-hide\" style=\"display:none;\">Toggle<\/span><span class=\"ez-toc-icon-toggle-span\"><svg style=\"fill: #999;color:#999\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewBox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #999;color:#999\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewBox=\"0 0 24 24\" version=\"1.2\" baseProfile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n<nav><ul class='ez-toc-list ez-toc-list-level-1 ' ><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Quick_Answer_CDSCO_Registration_for_Disposable_Medical_Devices_at_a_Glance\" title=\"Quick Answer: CDSCO Registration for Disposable Medical Devices at a Glance\">Quick Answer: CDSCO Registration for Disposable Medical Devices at a Glance<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#What_Is_CDSCO_Registration_for_Disposable_Medical_Devices\" title=\"What Is CDSCO Registration for Disposable Medical Devices?\">What Is CDSCO Registration for Disposable Medical Devices?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Are_Disposable_Medical_Devices_Regulated_by_CDSCO_in_India\" title=\"Are Disposable Medical Devices Regulated by CDSCO in India?\">Are Disposable Medical Devices Regulated by CDSCO in India?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#CDSCO_Medical_Device_Classification_for_Disposable_Devices\" title=\"CDSCO Medical Device Classification for Disposable Devices\">CDSCO Medical Device Classification for Disposable Devices<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Class_A_Disposable_Medical_Devices\" title=\"Class A Disposable Medical Devices\">Class A Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-6\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Class_B_Disposable_Medical_Devices\" title=\"Class B Disposable Medical Devices\">Class B Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-7\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Class_C_Disposable_Medical_Devices\" title=\"Class C Disposable Medical Devices\">Class C Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Class_D_Disposable_Medical_Devices\" title=\"Class D Disposable Medical Devices\">Class D Disposable Medical Devices<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-9\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Who_Needs_CDSCO_Registration_for_Disposable_Medical_Devices\" title=\"Who Needs CDSCO Registration for Disposable Medical Devices?\">Who Needs CDSCO Registration for Disposable Medical Devices?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-10\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Eligibility_for_CDSCO_Registration_of_Disposable_Medical_Devices\" title=\"Eligibility for CDSCO Registration of Disposable Medical Devices\">Eligibility for CDSCO Registration of Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-11\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#CDSCO_Registration_Process_for_Disposable_Medical_Devices_in_India\" title=\"CDSCO Registration Process for Disposable Medical Devices in India\">CDSCO Registration Process for Disposable Medical Devices in India<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-12\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Step_1_Identify_and_Classify_the_Medical_Device\" title=\"Step 1: Identify and Classify the Medical Device\">Step 1: Identify and Classify the Medical Device<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-13\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Step_2_Determine_the_Applicable_Regulatory_Route\" title=\"Step 2: Determine the Applicable Regulatory Route\">Step 2: Determine the Applicable Regulatory Route<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-14\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Step_3_Prepare_the_Required_Documents\" title=\"Step 3: Prepare the Required Documents\">Step 3: Prepare the Required Documents<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-15\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Step_4_Submit_the_Application\" title=\"Step 4: Submit the Application\">Step 4: Submit the Application<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-16\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Step_5_CDSCO_Review_and_Query_Resolution\" title=\"Step 5: CDSCO Review and Query Resolution\">Step 5: CDSCO Review and Query Resolution<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-17\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Step_6_Obtain_the_Applicable_Licence_or_Approval\" title=\"Step 6: Obtain the Applicable Licence or Approval\">Step 6: Obtain the Applicable Licence or Approval<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-18\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Documents_Required_for_CDSCO_Registration\" title=\"Documents Required for CDSCO Registration\">Documents Required for CDSCO Registration<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-19\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#CDSCO_Fees_for_Disposable_Medical_Device_Registration\" title=\"CDSCO Fees for Disposable Medical Device Registration\">CDSCO Fees for Disposable Medical Device Registration<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-20\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#CDSCO_Requirements_for_Disposable_Medical_Devices\" title=\"CDSCO Requirements for Disposable Medical Devices\">CDSCO Requirements for Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-21\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#CDSCO_Registration_for_Imported_Disposable_Medical_Devices\" title=\"CDSCO Registration for Imported Disposable Medical Devices\">CDSCO Registration for Imported Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-22\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#CDSCO_Registration_for_Indian_Manufacturers\" title=\"CDSCO Registration for Indian Manufacturers\">CDSCO Registration for Indian Manufacturers<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-23\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Labelling_and_Packaging_Requirements_for_Disposable_Medical_Devices\" title=\"Labelling and Packaging Requirements for Disposable Medical Devices\">Labelling and Packaging Requirements for Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-24\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Testing_and_Quality_Management_Requirements\" title=\"Testing and Quality Management Requirements\">Testing and Quality Management Requirements<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-25\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#CDSCO_Registration_Timeline_for_Disposable_Medical_Devices\" title=\"CDSCO Registration Timeline for Disposable Medical Devices\">CDSCO Registration Timeline for Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-26\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Common_Reasons_for_CDSCO_Application_Rejection_or_Delay\" title=\"Common Reasons for CDSCO Application Rejection or Delay\">Common Reasons for CDSCO Application Rejection or Delay<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-27\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Post-Registration_Compliance_for_Disposable_Medical_Devices\" title=\"Post-Registration Compliance for Disposable Medical Devices\">Post-Registration Compliance for Disposable Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-28\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#CDSCO_Registration_vs_CDSCO_Import_Licence\" title=\"CDSCO Registration vs CDSCO Import Licence\">CDSCO Registration vs CDSCO Import Licence<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-29\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Why_Choose_LegalRaasta_for_CDSCO_Registration\" title=\"Why Choose LegalRaasta for CDSCO Registration?\">Why Choose LegalRaasta for CDSCO Registration?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-30\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Conclusion\" title=\"Conclusion\">Conclusion<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-31\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#Frequently_Asked_Questions_FAQs\" title=\"Frequently Asked Questions (FAQs)\">Frequently Asked Questions (FAQs)<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-32\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#1_Does_every_disposable_product_need_CDSCO_Registration_for_Disposable_Medical_Devices\" title=\"1. Does every disposable product need CDSCO Registration for Disposable Medical Devices?\">1. Does every disposable product need CDSCO Registration for Disposable Medical Devices?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-33\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#2_What_is_a_medical_device_manufacturing_license_used_for\" title=\"2. What is a medical device manufacturing license used for?\">2. What is a medical device manufacturing license used for?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-34\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#3_How_long_does_CDSCO_Registration_for_Disposable_Medical_Devices_actually_take\" title=\"3. How long does CDSCO Registration for Disposable Medical Devices actually take?\">3. How long does CDSCO Registration for Disposable Medical Devices actually take?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-35\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#4_What_is_a_CDSCO_import_license_needed_for\" title=\"4. What is a CDSCO import license needed for?\">4. What is a CDSCO import license needed for?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-36\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#5_Can_foreign_manufacturers_apply_for_CDSCO_Registration_for_Disposable_Medical_Devices_directly\" title=\"5. Can foreign manufacturers apply for CDSCO Registration for Disposable Medical Devices directly?\">5. Can foreign manufacturers apply for CDSCO Registration for Disposable Medical Devices directly?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-37\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#6_What_is_Class_A_medical_device_classification_based_on\" title=\"6. What is Class A medical device classification based on?\">6. What is Class A medical device classification based on?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-38\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#7_Is_CDSCO_Registration_for_Disposable_Medical_Devices_mandatory_for_hospitals_selling_disposables\" title=\"7. Is CDSCO Registration for Disposable Medical Devices mandatory for hospitals selling disposables?\">7. Is CDSCO Registration for Disposable Medical Devices mandatory for hospitals selling disposables?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-39\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#8_What_happens_if_CDSCO_Registration_for_Disposable_Medical_Devices_is_skipped\" title=\"8. What happens if CDSCO Registration for Disposable Medical Devices is skipped?\">8. What happens if CDSCO Registration for Disposable Medical Devices is skipped?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-40\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#9_Does_CDSCO_Registration_for_Disposable_Medical_Devices_cover_both_manufacturing_and_import\" title=\"9. Does CDSCO Registration for Disposable Medical Devices cover both manufacturing and import?\">9. Does CDSCO Registration for Disposable Medical Devices cover both manufacturing and import?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-41\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#10_How_often_does_CDSCO_Registration_for_Disposable_Medical_Devices_need_renewal\" title=\"10. How often does CDSCO Registration for Disposable Medical Devices need renewal?\">10. How often does CDSCO Registration for Disposable Medical Devices need renewal?<\/a><\/li><\/ul><\/li><\/ul><\/nav><\/div>\n<h2><span class=\"ez-toc-section\" id=\"Quick_Answer_CDSCO_Registration_for_Disposable_Medical_Devices_at_a_Glance\"><\/span><b>Quick Answer: CDSCO Registration for Disposable Medical Devices at a Glance<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<table>\n<tbody>\n<tr>\n<td>\n<p><b>Requirement<\/b><\/p>\n<\/td>\n<td>\n<p><b>Details<\/b><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Regulator<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">CDSCO, under the Ministry of Health and Family Welfare<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Governing law<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Medical Devices Rules, 2017 (MDR 2017)<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Application portal<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">SUGAM (sugam.gov.in \/ <\/span><a href=\"http:\/\/cdscomdonline.gov.in\"><span style=\"font-weight: 400\">cdscomdonline.gov.in<\/span><\/a><span style=\"font-weight: 400\">)<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Manufacturing forms<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-3 \u2192 MD-5 (Class A\/B), MD-7 \u2192 MD-9 (Class C\/D)<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Import forms<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-14 \u2192 MD-15, via Indian Authorised Agent<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Manufacturing licence fee<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Rs 5,000 + Rs 500\/device (A\/B), Rs 50,000 + Rs 1,000\/device (C\/D)<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Import licence fee<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Roughly Rs 83,300 per site (A\/B), Rs 2,49,900 per site (C\/D), plus USD 1,000 per product<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Licence validity<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">5 years, renewable<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Processing time<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">3 to 6 months (A\/B), 9 to 18 months (C\/D)<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2><span class=\"ez-toc-section\" id=\"What_Is_CDSCO_Registration_for_Disposable_Medical_Devices\"><\/span><b>What Is CDSCO Registration for Disposable Medical Devices?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">CDSCO Registration for Disposable Medical Devices is the licence that lets you legally manufacture, import, sell, or distribute single-use medical products in India.<\/span><\/p>\n<p><span style=\"font-weight: 400\">It applies to items used once and discarded, such as syringes, gloves, catheters, IV sets, dressings, and dozens of similar products. Without the CDSCO licence, you can&#8217;t sell the product to a hospital, list it on a government e-procurement portal, or clear it through Indian customs if you import it.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Are_Disposable_Medical_Devices_Regulated_by_CDSCO_in_India\"><\/span><b>Are Disposable Medical Devices Regulated by CDSCO in India?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Yes, and this wasn&#8217;t always the case. Before 2020, only a limited list of notified devices needed CDSCO approval. A government notification, S.O. 648(E), brought every medical device, disposable or otherwise, under regulation from April 2020, rolled out in phases by risk class.<\/span><\/p>\n<p><span style=\"font-weight: 400\">So today, if your product meets the legal definition of a medical device under the Drugs and Cosmetics Act, it needs CDSCO clearance. There&#8217;s one exception worth knowing. Class A devices that are non-sterile and non-measuring were exempted from mandatory licensing under a 2026 CDSCO update, though they still need registration on the portal.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"CDSCO_Medical_Device_Classification_for_Disposable_Devices\"><\/span><b>CDSCO Medical Device Classification for Disposable Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Classification decides everything that follows: which form you file, how much you pay, and how long approval takes. Here&#8217;s how disposable products typically fall across the four risk classes.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Class_A_Disposable_Medical_Devices\"><\/span><b>Class A Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Lowest risk. Examples include examination gloves, gauze, cotton swabs, alcohol swabs, disposable face masks, and tongue depressors. Many now only need registration, not a full licence, under the 2026 NSNM exemption.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Class_B_Disposable_Medical_Devices\"><\/span><b>Class B Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Low to moderate risk. Disposable syringes, hypodermic needles, IV cannulas, urine bags, Foley catheters and disposable scalp vein sets sit here. A full manufacturing or import licence is mandatory.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Class_C_Disposable_Medical_Devices\"><\/span><b>Class C Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Moderate to high risk. Disposable dialyser sets, blood tubing sets for haemodialysis, and certain drug-delivery catheters fall in this bracket. Expect stricter documentation and a site inspection.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Class_D_Disposable_Medical_Devices\"><\/span><b>Class D Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Highest risk. Disposable devices used in critical or cardiac care, angiography catheters being one example, attract the most rigorous CDSCO review, including clinical data in some cases.<\/span><\/p>\n<p><b>Always confirm your specific product against CDSCO&#8217;s official classification list before filing.<\/b><span style=\"font-weight: 400\"> Misclassification is the single biggest cause of rejected applications.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Who_Needs_CDSCO_Registration_for_Disposable_Medical_Devices\"><\/span><b>Who Needs CDSCO Registration for Disposable Medical Devices?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Anyone touching the product commercially needs to be on record with CDSCO. That includes Indian manufacturers producing disposables domestically, foreign manufacturers exporting into India through an Indian Authorised Agent, importers and distributors who stock and resell devices, and contract manufacturers who assemble, sterilise or repackage devices in India, even from imported components.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Eligibility_for_CDSCO_Registration_of_Disposable_Medical_Devices\"><\/span><b>Eligibility for CDSCO Registration of Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">You need a valid <\/span><a href=\"https:\/\/www.legalraasta.com\/private-limited-company-registration\/\"><span style=\"font-weight: 400\">business entity registered<\/span><\/a><span style=\"font-weight: 400\"> in India, a <\/span><a href=\"https:\/\/www.legalraasta.com\/gst-registration\/\"><span style=\"font-weight: 400\">GST registration<\/span><\/a><span style=\"font-weight: 400\">, and for manufacturers, premises that meet the Fifth Schedule quality management requirements under MDR 2017. Foreign manufacturers without an Indian office must appoint an Indian Authorised Agent holding a wholesale licence in Form MD-42 before they can even begin the SUGAM application.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"CDSCO_Registration_Process_for_Disposable_Medical_Devices_in_India\"><\/span><b>CDSCO Registration Process for Disposable Medical Devices in India<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">The process runs through six broad stages, though the exact paperwork changes depending on whether you manufacture in India or import.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Step_1_Identify_and_Classify_the_Medical_Device\"><\/span><b>Step 1: Identify and Classify the Medical Device<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Check your product against CDSCO&#8217;s classification list first. Everything downstream- the form, the fee, the timeline- depends on getting this right.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Step_2_Determine_the_Applicable_Regulatory_Route\"><\/span><b>Step 2: Determine the Applicable Regulatory Route<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Decide whether you need MD-3\/MD-5 (manufacturing, Class A\/B), MD-7\/MD-9 (manufacturing, Class C\/D), or MD-14\/MD-15 (import, any class).<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Step_3_Prepare_the_Required_Documents\"><\/span><b>Step 3: Prepare the Required Documents<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Compile the Device Master File, Plant Master File, quality management certificates, and labelling artwork. This step usually takes the longest, so start early.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Step_4_Submit_the_Application\"><\/span><b>Step 4: Submit the Application<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">File through the SUGAM portal at <\/span><a href=\"http:\/\/sugam.gov.in\"><span style=\"font-weight: 400\">sugam.gov.in<\/span><\/a><span style=\"font-weight: 400\">. Offline or physical submissions are not accepted for any category.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Step_5_CDSCO_Review_and_Query_Resolution\"><\/span><b>Step 5: CDSCO Review and Query Resolution<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">A reviewing officer examines the application and raises queries if anything is missing. Class C and D applications may also involve a physical site inspection.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Step_6_Obtain_the_Applicable_Licence_or_Approval\"><\/span><b>Step 6: Obtain the Applicable Licence or Approval<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Once cleared, you receive Form MD-5, MD-9, or MD-15 depending on your category, valid for five years from the date of issue.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Documents_Required_for_CDSCO_Registration\"><\/span><b>Documents Required for CDSCO Registration<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<table>\n<tbody>\n<tr>\n<td>\n<p><b>Document<\/b><\/p>\n<\/td>\n<td>\n<p><b>Manufacturer<\/b><\/p>\n<\/td>\n<td>\n<p><b>Importer<\/b><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Device Master File<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Plant Master File<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes (foreign site)<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">ISO 13485 certificate<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes, from foreign site<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Free Sale Certificate<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Not applicable<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes, from country of origin<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Constitution\/<\/span><a href=\"https:\/\/www.legalraasta.com\/llp-registration\/\"><span style=\"font-weight: 400\">incorporation documents<\/span><\/a><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Power of Attorney for Indian Authorised Agent<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Not applicable<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Wholesale licence (Form MD-42) of the agent<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Not applicable<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Labelling and Instructions for Use, in English\/Hindi<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Yes<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2><span class=\"ez-toc-section\" id=\"CDSCO_Fees_for_Disposable_Medical_Device_Registration\"><\/span><b>CDSCO Fees for Disposable Medical Device Registration<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Fees scale sharply with device class, and manufacturing costs are far less than importing.<\/span><\/p>\n<table>\n<tbody>\n<tr>\n<td>\n<p><b>Category<\/b><\/p>\n<\/td>\n<td>\n<p><b>Application<\/b><\/p>\n<\/td>\n<td>\n<p><b>Licence<\/b><\/p>\n<\/td>\n<td>\n<p><b>Site Fee<\/b><\/p>\n<\/td>\n<td>\n<p><b>Per-Device Fee<\/b><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Manufacturing, Class A\/B<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-3<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-5<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Rs 5,000<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Rs 500<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Manufacturing, Class C\/D<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-7<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-9<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Rs 50,000<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Rs 1,000<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Import, Class A\/B<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-14<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-15<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Approx. Rs 83,300<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">USD 1,000<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Import, Class C\/D<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-14<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-15<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Approx. Rs 2,49,900<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">USD 1,000<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"font-weight: 400\">These figures are indicative. Always verify the exact fee on the SUGAM portal before filing, since the Ministry revises the fee schedule from time to time.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"CDSCO_Requirements_for_Disposable_Medical_Devices\"><\/span><b>CDSCO Requirements for Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Beyond the licence itself, CDSCO expects a functioning quality management system aligned with the Fifth Schedule of MDR 2017, sterilisation validation for single-use sterile products, biocompatibility data where the device contacts skin or mucous membranes, and a documented risk management file. None of this is optional, even for a simple product like a disposable syringe.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"CDSCO_Registration_for_Imported_Disposable_Medical_Devices\"><\/span><b>CDSCO Registration for Imported Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Import approvals go through the Central Licensing Authority regardless of class, unlike manufacturing, where State Licensing Authorities handle Class A and B. The foreign manufacturer cannot apply directly. Their Indian Authorised Agent files Form MD-14 on their behalf, and once approved, the agent holds Form MD-15 and is responsible for customs clearance, post-market surveillance reporting, and adverse event tracking in India.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"CDSCO_Registration_for_Indian_Manufacturers\"><\/span><b>CDSCO Registration for Indian Manufacturers<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Domestic manufacturers deal with State Licensing Authorities for Class A and B disposables, which usually means faster turnaround and no mandatory site audit for Class A products. Class C and D manufacturing shifts to the Central Licensing Authority, the DCGI&#8217;s office in Delhi, and always involves a plant inspection before the licence is granted.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Labelling_and_Packaging_Requirements_for_Disposable_Medical_Devices\"><\/span><b>Labelling and Packaging Requirements for Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Every disposable device sold in India needs its CDSCO licence number, batch number, manufacturing and expiry dates, sterilisation status where applicable, and storage instructions printed clearly on the pack. Labels must carry information in English, and increasingly, Hindi is expected as well for products reaching government hospitals and rural markets. Single-use products additionally need a &#8220;Do Not Reuse&#8221; symbol or equivalent statement.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Testing_and_Quality_Management_Requirements\"><\/span><b>Testing and Quality Management Requirements<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Sterile disposables need sterilisation validation reports, usually from a NABL-accredited lab. Non-sterile Class A products face lighter testing, but biocompatibility and material safety data are still expected if the device touches the body. Your quality management system, whether it&#8217;s an in-house SOP framework or a full ISO 13485 certification, gets reviewed as part of the application, not after.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"CDSCO_Registration_Timeline_for_Disposable_Medical_Devices\"><\/span><b>CDSCO Registration Timeline for Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Class A and B manufacturing licences typically take 3 to 6 months from a complete application. Class C and D manufacturing can stretch to 9 to 18 months, mostly because of the mandatory site inspection and, sometimes, a technical committee review. Import licences follow a similar pattern: 6 to 12 months for Class A\/B, 9 to 15 months for Class C\/D, counted from the date the Indian Authorised Agent files Form MD-14.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Common_Reasons_for_CDSCO_Application_Rejection_or_Delay\"><\/span><b>Common Reasons for CDSCO Application Rejection or Delay<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<ul>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Wrong risk classification claimed at the outset<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Incomplete Device Master File or missing sterilisation validation data<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Labelling that doesn&#8217;t match the approved product description<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Foreign manufacturer applying directly instead of through an Indian Authorised Agent<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Expired or mismatched ISO 13485 certification<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Fee challan errors or payment made outside the SUGAM portal<\/span><\/li>\n<\/ul>\n<h2><span class=\"ez-toc-section\" id=\"Post-Registration_Compliance_for_Disposable_Medical_Devices\"><\/span><b>Post-Registration Compliance for Disposable Medical Devices<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">The licence isn&#8217;t the finish line. Manufacturers and importers must track adverse events and report them to CDSCO, maintain batch records for traceability, renew the licence before the five-year validity lapses, and inform CDSCO of any change in manufacturing site, product specification, or Indian Authorised Agent. Skipping renewal is one of the most common ways companies lose their market access overnight.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"CDSCO_Registration_vs_CDSCO_Import_Licence\"><\/span><b>CDSCO Registration vs CDSCO Import Licence<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<table>\n<tbody>\n<tr>\n<td>\n<p><b>Point<\/b><\/p>\n<\/td>\n<td>\n<p><b>CDSCO Registration<\/b><\/p>\n<\/td>\n<td>\n<p><b>CDSCO Import Licence<\/b><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Applies to<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Class A NSNM devices, domestic products in general<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">All imported medical devices<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Form<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Registration on SUGAM portal<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">MD-14 (application), MD-15 (licence)<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Who applies<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Manufacturer or entity directly<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Indian Authorised Agent, on behalf of foreign manufacturer<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Site inspection<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Rarely required<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Common for Class C\/D<\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<p><span style=\"font-weight: 400\">Typical use case<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Low-risk domestic disposables<\/span><\/p>\n<\/td>\n<td>\n<p><span style=\"font-weight: 400\">Foreign-manufactured devices entering India<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2><span class=\"ez-toc-section\" id=\"Why_Choose_LegalRaasta_for_CDSCO_Registration\"><\/span><b>Why Choose LegalRaasta for CDSCO Registration?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">Getting classification wrong once means restarting the entire filing, and that costs months, not days. LegalRaasta&#8217;s regulatory team classifies your disposable device correctly, builds the Device Master File, handles the SUGAM filing end to end, and follows up on CDSCO queries so your licence doesn&#8217;t sit stuck for six extra months over a document you could have fixed upfront.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Conclusion\"><\/span><b>Conclusion<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-weight: 400\">CDSCO Registration for Disposable Medical Devices isn&#8217;t a one-size-fits-all process. A box of examination gloves and a haemodialysis set follow completely different paths, timelines, and fee structures. What stays constant is this: get the classification right, keep the documentation airtight, and file through the correct route the first time. Reach out to LegalRaasta to get your disposable medical device registered without the back and forth.<\/span><\/p>\n<h2><span class=\"ez-toc-section\" id=\"Frequently_Asked_Questions_FAQs\"><\/span><b>Frequently Asked Questions (FAQs)<\/b><span class=\"ez-toc-section-end\"><\/span><\/h2>\n<h3><span class=\"ez-toc-section\" id=\"1_Does_every_disposable_product_need_CDSCO_Registration_for_Disposable_Medical_Devices\"><\/span><b>1. Does every disposable product need CDSCO Registration for Disposable Medical Devices?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Almost all do. Even low-risk Class A medical device items like gauze or gloves need registration, though some non-sterile ones are now exempt from full licensing.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"2_What_is_a_medical_device_manufacturing_license_used_for\"><\/span><b>2. What is a medical device manufacturing license used for?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">It&#8217;s the legal permission to produce devices in India. For CDSCO Registration for Disposable Medical Devices, manufacturers file Form MD-3 or MD-7 depending on risk class.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"3_How_long_does_CDSCO_Registration_for_Disposable_Medical_Devices_actually_take\"><\/span><b>3. How long does CDSCO Registration for Disposable Medical Devices actually take?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Class A and B products usually clear in 3 to 6 months. Class C and D can take 9 to 18 months because of mandatory site inspections under SUGAM portal registration.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"4_What_is_a_CDSCO_import_license_needed_for\"><\/span><b>4. What is a CDSCO import license needed for?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">It authorises bringing foreign-made devices into India. Foreign firms outside the CDSCO Registration for Disposable Medical Devices rules must use an Indian Authorised Agent to import legally.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"5_Can_foreign_manufacturers_apply_for_CDSCO_Registration_for_Disposable_Medical_Devices_directly\"><\/span><b>5. Can foreign manufacturers apply for CDSCO Registration for Disposable Medical Devices directly?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">No, they cannot. Only an Indian Authorised Agent, holding a valid wholesale licence, can file the SUGAM portal registration on their behalf.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"6_What_is_Class_A_medical_device_classification_based_on\"><\/span><b>6. What is Class A medical device classification based on?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">It&#8217;s based on risk to the patient, the lowest tier. CDSCO Registration for Disposable Medical Devices treats Class A items like masks and swabs with the lightest scrutiny.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"7_Is_CDSCO_Registration_for_Disposable_Medical_Devices_mandatory_for_hospitals_selling_disposables\"><\/span><b>7. Is CDSCO Registration for Disposable Medical Devices mandatory for hospitals selling disposables?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Hospitals using devices don&#8217;t need the licence themselves, but any manufacturer or importer supplying them under medical device classification in India rules absolutely does.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"8_What_happens_if_CDSCO_Registration_for_Disposable_Medical_Devices_is_skipped\"><\/span><b>8. What happens if CDSCO Registration for Disposable Medical Devices is skipped?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Products get seized at customs or during inspection, and penalties follow under the Drugs and Cosmetics Act, alongside the loss of a valid medical device manufacturing license.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"9_Does_CDSCO_Registration_for_Disposable_Medical_Devices_cover_both_manufacturing_and_import\"><\/span><b>9. Does CDSCO Registration for Disposable Medical Devices cover both manufacturing and import?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Yes, it covers both, just through different forms: MD-3\/MD-7 for domestic manufacturing and the CDSCO import license route for foreign-made devices.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"10_How_often_does_CDSCO_Registration_for_Disposable_Medical_Devices_need_renewal\"><\/span><b>10. How often does CDSCO Registration for Disposable Medical Devices need renewal?<\/b><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-weight: 400\">Every five years. Missing renewal under the SUGAM portal registration means the licence lapses, and the product can no longer be legally sold in India.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Selling syringes, gloves, or IV sets in India without a licence sounds harmless. It isn&#8217;t. CDSCO Registration for Disposable Medical Devices is a legal requirement, not paperwork you can skip and fix later. Miss it, and customs holds your shipment or a state drug inspector shuts your unit down mid-production. Get it right the first time, [&hellip;]<\/p>\n","protected":false},"author":15,"featured_media":36567,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[5155],"tags":[],"class_list":["post-36566","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-cdsco"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>CDSCO Registration for Disposable Medical Devices in India<\/title>\n<meta name=\"description\" content=\"CDSCO registration for disposable medical devices in India, including eligibility, process, documents, fees, classification, and compliance.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"CDSCO Registration for Disposable Medical Devices in India\" \/>\n<meta property=\"og:description\" content=\"CDSCO registration for disposable medical devices in India, including eligibility, process, documents, fees, classification, and compliance.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/\" \/>\n<meta property=\"og:site_name\" content=\"LegalRaasta Knowledge portal\" \/>\n<meta property=\"article:published_time\" content=\"2026-08-31T06:43:11+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1280\" \/>\n\t<meta property=\"og:image:height\" content=\"675\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Author: LegalRaasta\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Author: LegalRaasta\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"10 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/\"},\"author\":{\"name\":\"Author: LegalRaasta\",\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/#\\\/schema\\\/person\\\/8fffceba7148ae1120f0bd4bf73b0c62\"},\"headline\":\"CDSCO Registration for Disposable Medical Devices in India: Eligibility, Process, Documents, Fees &amp; Compliance\",\"datePublished\":\"2026-08-31T06:43:11+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/\"},\"wordCount\":2181,\"image\":{\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg\",\"articleSection\":[\"CDSCO\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/\",\"url\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/\",\"name\":\"CDSCO Registration for Disposable Medical Devices in India\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg\",\"datePublished\":\"2026-08-31T06:43:11+00:00\",\"author\":{\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/#\\\/schema\\\/person\\\/8fffceba7148ae1120f0bd4bf73b0c62\"},\"description\":\"CDSCO registration for disposable medical devices in India, including eligibility, process, documents, fees, classification, and compliance.\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/#primaryimage\",\"url\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg\",\"contentUrl\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg\",\"width\":1280,\"height\":675,\"caption\":\"CDSCO Registration for Disposable Medical Devices\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/cdsco-registration-for-disposable-medical-devices\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"CDSCO\",\"item\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/category\\\/cdsco\\\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"CDSCO Registration for Disposable Medical Devices in India: Eligibility, Process, Documents, Fees &amp; Compliance\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/#website\",\"url\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/\",\"name\":\"LegalRaasta Knowledge portal\",\"description\":\"Information on company registration, FSSAI, IEC, MSME, trademark, ISO and registrations\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/#\\\/schema\\\/person\\\/8fffceba7148ae1120f0bd4bf73b0c62\",\"name\":\"Author: LegalRaasta\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/wp-content\\\/uploads\\\/2026\\\/03\\\/author-legalraasta_avatar_1-96x96.png\",\"url\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/wp-content\\\/uploads\\\/2026\\\/03\\\/author-legalraasta_avatar_1-96x96.png\",\"contentUrl\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/wp-content\\\/uploads\\\/2026\\\/03\\\/author-legalraasta_avatar_1-96x96.png\",\"caption\":\"Author: LegalRaasta\"},\"description\":\"LegalRaasta is one of India\u2019s leading platforms for Company Registration (Private Limited, LLP, OPC) and GST compliance. Since 2015, our team of experienced CAs and legal experts has assisted over 100,000 businesses with services like Trademark, FSSAI, BIS, and Startup India registration. We simplify complex government processes to help startups and entrepreneurs grow faster. Trusted across India, LegalRaasta makes legal and financial compliance simple, quick, and affordable.\",\"url\":\"https:\\\/\\\/www.legalraasta.com\\\/blog\\\/author\\\/adarshseoexecutive\\\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"CDSCO Registration for Disposable Medical Devices in India","description":"CDSCO registration for disposable medical devices in India, including eligibility, process, documents, fees, classification, and compliance.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/","og_locale":"en_US","og_type":"article","og_title":"CDSCO Registration for Disposable Medical Devices in India","og_description":"CDSCO registration for disposable medical devices in India, including eligibility, process, documents, fees, classification, and compliance.","og_url":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/","og_site_name":"LegalRaasta Knowledge portal","article_published_time":"2026-08-31T06:43:11+00:00","og_image":[{"width":1280,"height":675,"url":"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg","type":"image\/jpeg"}],"author":"Author: LegalRaasta","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Author: LegalRaasta","Est. reading time":"10 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#article","isPartOf":{"@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/"},"author":{"name":"Author: LegalRaasta","@id":"https:\/\/www.legalraasta.com\/blog\/#\/schema\/person\/8fffceba7148ae1120f0bd4bf73b0c62"},"headline":"CDSCO Registration for Disposable Medical Devices in India: Eligibility, Process, Documents, Fees &amp; Compliance","datePublished":"2026-08-31T06:43:11+00:00","mainEntityOfPage":{"@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/"},"wordCount":2181,"image":{"@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#primaryimage"},"thumbnailUrl":"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg","articleSection":["CDSCO"],"inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/","url":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/","name":"CDSCO Registration for Disposable Medical Devices in India","isPartOf":{"@id":"https:\/\/www.legalraasta.com\/blog\/#website"},"primaryImageOfPage":{"@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#primaryimage"},"image":{"@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#primaryimage"},"thumbnailUrl":"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg","datePublished":"2026-08-31T06:43:11+00:00","author":{"@id":"https:\/\/www.legalraasta.com\/blog\/#\/schema\/person\/8fffceba7148ae1120f0bd4bf73b0c62"},"description":"CDSCO registration for disposable medical devices in India, including eligibility, process, documents, fees, classification, and compliance.","breadcrumb":{"@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/"]}]},{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#primaryimage","url":"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg","contentUrl":"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/08\/CDSCO-Registration-for-Disposable-Medical-Devices.jpg","width":1280,"height":675,"caption":"CDSCO Registration for Disposable Medical Devices"},{"@type":"BreadcrumbList","@id":"https:\/\/www.legalraasta.com\/blog\/cdsco-registration-for-disposable-medical-devices\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.legalraasta.com\/blog\/"},{"@type":"ListItem","position":2,"name":"CDSCO","item":"https:\/\/www.legalraasta.com\/blog\/category\/cdsco\/"},{"@type":"ListItem","position":3,"name":"CDSCO Registration for Disposable Medical Devices in India: Eligibility, Process, Documents, Fees &amp; Compliance"}]},{"@type":"WebSite","@id":"https:\/\/www.legalraasta.com\/blog\/#website","url":"https:\/\/www.legalraasta.com\/blog\/","name":"LegalRaasta Knowledge portal","description":"Information on company registration, FSSAI, IEC, MSME, trademark, ISO and registrations","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.legalraasta.com\/blog\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Person","@id":"https:\/\/www.legalraasta.com\/blog\/#\/schema\/person\/8fffceba7148ae1120f0bd4bf73b0c62","name":"Author: LegalRaasta","image":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/03\/author-legalraasta_avatar_1-96x96.png","url":"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/03\/author-legalraasta_avatar_1-96x96.png","contentUrl":"https:\/\/www.legalraasta.com\/blog\/wp-content\/uploads\/2026\/03\/author-legalraasta_avatar_1-96x96.png","caption":"Author: LegalRaasta"},"description":"LegalRaasta is one of India\u2019s leading platforms for Company Registration (Private Limited, LLP, OPC) and GST compliance. Since 2015, our team of experienced CAs and legal experts has assisted over 100,000 businesses with services like Trademark, FSSAI, BIS, and Startup India registration. We simplify complex government processes to help startups and entrepreneurs grow faster. Trusted across India, LegalRaasta makes legal and financial compliance simple, quick, and affordable.","url":"https:\/\/www.legalraasta.com\/blog\/author\/adarshseoexecutive\/"}]}},"_links":{"self":[{"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/posts\/36566","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/users\/15"}],"replies":[{"embeddable":true,"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/comments?post=36566"}],"version-history":[{"count":1,"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/posts\/36566\/revisions"}],"predecessor-version":[{"id":36568,"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/posts\/36566\/revisions\/36568"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/media\/36567"}],"wp:attachment":[{"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/media?parent=36566"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/categories?post=36566"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.legalraasta.com\/blog\/wp-json\/wp\/v2\/tags?post=36566"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}