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/2019/000021_76dd9d462e9ff1c1fe9da2d50679fb98_6f9b5220145333a7bb21b8241c815004. This device is marketed under the brand name Multiverse. The license holder is Dolphin Lifescience India LLP, 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/2019/000021_76dd9d462e9ff1c1fe9da2d50679fb98_6f9b5220145333a7bb21b8241c815004

Brand Name

Multiverse

Device Class

Class B

Approving Authority

Gujarat

Product Information

Manifold is an accessory design to facilitate the directional control of fluid material used in conjunction with interventional devices during vascular interventional procedures.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing