CDSCO legacy medical-device registration POA model
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
Legacy power-of-attorney model for medical-device registration certificates under the 1945 Rules is published by Central Drugs Standard Control Organization. This document is identified by its title; no separate official document code is recorded.
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- CDSCO legacy medical-device registration POA model
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- Registration
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Legacy power-of-attorney model for medical-device registration certificates under the 1945 Rules
Complete 3-page legacy blank official power-of-attorney model for medical-device Registration Certificates under the Drugs and Cosmetics Rules 1945, including original change-reporting declarations, device/model schedule and manufacturer/Indian-agent signature fields. Mixed legacy drug/device terminology and references remain as printed. No issue or effective date is established. This is not an MDR 2017 Subsequent Importer checklist or evidence of current model requirements, deadlines or fees. Scope is the expressly named medical-device legacy form; no automatic IVD extension. Complete original page images govern; native extraction is a qualified, potentially incomplete search layer. No whole-country completeness or completed-question claim.
This document is identified by its title; no separate official document code is recorded. Always confirm the current consolidated text and transition provisions with the official source before filing.