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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/2021/000044_76dd9d462e9ff1c1fe9da2d50679fb98_5476fac6e702dd0e46cea35940c6d0f1. This device is marketed under the brand name Trans-Needle . The license holder is Translumina Therapeutics LLP, 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
Manifold
UID: MFG/MD/2021/000044_76dd9d462e9ff1c1fe9da2d50679fb98_5476fac6e702dd0e46cea35940c6d0f1

Brand Name

Trans-Needle

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

Trans-Fold is intended for connection between the devices, such like injection syringe, angiographic catheter, drip set to the bottle delivering contrast agent or saline flush, or pressure monitoring system, etc. Each fluid channels can be independently controlled by switch

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