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RFS - India CDSCO Medical Device Registration

RFS is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000003_d1352e251a6f312021f06291e1547853_681ca3208d17cf15742f651164b12d20. This device is marketed under the brand name 3 Part Differential. The license holder is Avantor Performance Materials India Limited, and it is classified as Device Class Class B. The approving authority is Uttarakhand.

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
RFS
UID: MFG/IVD/2020/000003_d1352e251a6f312021f06291e1547853_681ca3208d17cf15742f651164b12d20

Brand Name

3 Part Differential

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

Determination of RF factor in Human Serum

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