Pure Global

Bipolar Arthroscopic RF System - India CDSCO Medical Device Registration

Bipolar Arthroscopic RF System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000152_1e4ae5a85734d6c31340d7cc2ebb1b5c_689b8f735fbcaab18886791005deec24. This device is marketed under the brand name GenesysMatryx Interference Screw. The license holder is M/s Linvatec India Private Limited, and it is classified as Device Class Class D. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class D
Bipolar Arthroscopic RF System
UID: IMP/MD/2019/000152_1e4ae5a85734d6c31340d7cc2ebb1b5c_689b8f735fbcaab18886791005deec24

Brand Name

GenesysMatryx Interference Screw

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Arthroscopic Energy System is indicated for resection, ablation, and coagulation of tissue and haemostasis of blood vessels in arthroscopic and orthopaedic surgical procedures.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing