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Tubing - India CDSCO Medical Device Registration

Tubing is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000458_f12a102010db39a07d47699f4787f7ea_18d1289b8548cb70a553afc821a1ed44. This device is marketed under the brand name FMS VUE II . The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

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
Tubing
UID: IMP/MD/2019/000458_f12a102010db39a07d47699f4787f7ea_18d1289b8548cb70a553afc821a1ed44

Brand Name

FMS VUE II

Device Class

Class B

Approving Authority

CDSCO

Product Information

The FMS VUE II Fluid Management and Tissue Debridement System is intended to provide controlled fluid distention and suction, controlled cutting, burring, shaving and abrading of bone and tissue for use in arthroscopic surgery of the shoulder, knee, ankle, elbow, wrist and hip joints

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