3 Port Manifold Kit - India CDSCO Medical Device Registration

3 Port Manifold Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000130_84fd7f4784c3386e9c2e5ec1193aa1ca_55fc3982e5743f6fc44ffc7c5533da04. This device is marketed under the brand name Flexoline. The license holder is George Philips Medical Engineering Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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CDSCO Registered

Class Class B

3 Port Manifold Kit

UID: MFG/MD/2022/000130_84fd7f4784c3386e9c2e5ec1193aa1ca_55fc3982e5743f6fc44ffc7c5533da04

Brand Name

Flexoline

License Holder

George Philips Medical Engineering Pvt Ltd

Device Class

Class B

Approving Authority

Kokan Division

Product Information

3 Port Manifold Kits are intended to be used to establish connections between equipment’s and physiological monitoring equipment’s to monitor infusion and physiques

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Extension Line With Needle Less Connector

Brand: Flexoline

George Philips Medical Engineering Pvt Ltd

3 Port Manifold Kit - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

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