Pure Global

Manifold - India CDSCO Medical Device Registration

Manifold is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000111_76dd9d462e9ff1c1fe9da2d50679fb98_d4a658baa0b037c39fb944cbdef06ef1. The license holder is Advanced MedTech Solutions Private Limited, and it is classified as Device Class Class B. The approving authority is Gujarat.

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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Manifold
UID: MFG/MD/2022/000111_76dd9d462e9ff1c1fe9da2d50679fb98_d4a658baa0b037c39fb944cbdef06ef1

Device Class

Class B

Approving Authority

Gujarat

Product Information

Manifolds are used as an accessory intended to provide effective control on the rate and direction of the fluid flow during invasive and catheterization procedures

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing