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/2020/000118_76dd9d462e9ff1c1fe9da2d50679fb98_ddc2f9b81edc8ba0f645feb1d23f35b6. This device is marketed under the brand name GENTLE. The license holder is Relisys Medical Devices Limited, and it is classified as Device Class Class B. The approving authority is Telangana.

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CDSCO Registered

Class Class B

Manifold

UID: MFG/MD/2020/000118_76dd9d462e9ff1c1fe9da2d50679fb98_ddc2f9b81edc8ba0f645feb1d23f35b6

Brand Name

GENTLE

License Holder

Relisys Medical Devices Limited

Device Class

Class B

Approving Authority

Telangana

Product Information

Manifold is a kind of transfusion device, T shape with an ?off? right handle, can control the direction of flow of fluid, with the high pressure of 500PSI, this manifold generally used as an important accessory during the process of angiography operation or interventional operation. It will be innocuous disposed immediately after single use