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Central Venous Catheter Kit - India CDSCO Medical Device Registration

Central Venous Catheter Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000130_ceb9df1b3f5d1bccc1dfd8527cec4a75_7b1fd7380a13ec14d91f83505560833a. 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
Central Venous Catheter Kit
UID: MFG/MD/2022/000130_ceb9df1b3f5d1bccc1dfd8527cec4a75_7b1fd7380a13ec14d91f83505560833a

Brand Name

Flexoline

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Central Venous Catheter Kits are intended to be used by the single and multiple-lumen catheters that permit venous access to the adult and paediatric central circulation for the administration of medicines, blood sampling, and pressure monitoring

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