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Platelet Rich Plasma tube - India CDSCO Medical Device Registration

Platelet Rich Plasma tube is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000311_44a57afb382f943961cd4132402f2e1f_187cd0b9f95d889ef44b5874534465aa. This device is marketed under the brand name PRP. The license holder is Plot No 64/A & 68/A, Piparia Inductrial Estate, Dan Udyog, Piparia, Silavassa,396230 (UT Of DNH), and it is classified as Device Class Class B. The approving authority is Dadra And Nagar Haveli.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
Platelet Rich Plasma tube
UID: MFG/MD/2022/000311_44a57afb382f943961cd4132402f2e1f_187cd0b9f95d889ef44b5874534465aa

Brand Name

PRP

Device Class

Class B

Approving Authority

Dadra And Nagar Haveli

Product Information

Intended use is the preparation of Autologous Platelet Rich Plasma or other plasma derivatives.

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