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Coblation System - India CDSCO Medical Device Registration

Coblation System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000409_01fe644b80b158370ab3ce6b7a742d7e_dcc62820b0bd74f910c160d771f0359e. This device is marketed under the brand name WEREWOLF. The license holder is Smith & Nephew Healthcare Pvt. Ltd., and it is classified as Device Class Class C. 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 C
Coblation System
UID: IMP/MD/2021/000409_01fe644b80b158370ab3ce6b7a742d7e_dcc62820b0bd74f910c160d771f0359e

Brand Name

WEREWOLF

Device Class

Class C

Approving Authority

CDSCO

Product Information

The WEREWOLF COBLATION System controller is indicated for the resection, ablation, and coagulation of soft tissues and hemostasis of blood vessels in arthroscopic, orthopedic and otorhinolaryngology (WEREWOLF) procedures (WEREWOLF)

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