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Haemodialysis Catheter Kit - India CDSCO Medical Device Registration

Haemodialysis Catheter Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000130_71c3dabda74813a9e6006c41e28798b1_835c6808f27eafb052c3a51b2af7e195. 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.

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
Haemodialysis Catheter Kit
UID: MFG/MD/2022/000130_71c3dabda74813a9e6006c41e28798b1_835c6808f27eafb052c3a51b2af7e195

Brand Name

Flexoline

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Haemodialysis Catheter Kits are intended to be used for short-term venous access during haemodialysis, hemoperfusion, infusion and apheresis treatments

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