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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/2021/000261_76dd9d462e9ff1c1fe9da2d50679fb98_8f8ed130478e11df27c78e9645a3b9e6. This device is marketed under the brand name Trans PTCA Kit-Prime. The license holder is Microtrol Sterilisation Services Pvt Ltd., and it is classified as Device Class Class B. The approving authority is Haryana.

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/2021/000261_76dd9d462e9ff1c1fe9da2d50679fb98_8f8ed130478e11df27c78e9645a3b9e6

Brand Name

Trans PTCA Kit-Prime

Device Class

Class B

Approving Authority

Haryana

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

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