CDSCO UID MFG/MD/2022/000642_af248abf25630ef2d4a0fd6cdcab5c0d_c8bba31f9c496a60473d2f4988585fd9

Arthroscopy Implant

GMP Meditech·Device Class Class C·India CDSCO·Brand: Titanium
Registration details
UID
MFG/MD/2022/000642_af248abf25630ef2d4a0fd6cdcab5c0d_c8bba31f9c496a60473d2f4988585fd9
Device class
Class C
Brand name
Titanium
License holder
GMP Meditech
Approving authority
Central Drug Standards Control Organization, Ahmedabad
Product information
Arthroscopy Implants is intended to be used for the fixation of soft tissue fixation or anchorage
Similar products (10)
Other products with the same name or brand
Arthroscopy Implant
Brand: SS
Orthrex Life Care
Class C
Arthroscopy Implant
Brand: SS
Orthrex Life Care
Class C
Bone Screw
Brand: Titanium
GMP Meditech
Class C
Bone Screw
Brand: Titanium
GMP Meditech
Class C
Bone Nail
Brand: Titanium
GMP Meditech
Class C
Maxillofacial Implant
Brand: Titanium
GMP Meditech
Class C
Pins and Wires
Brand: Titanium
GMP Meditech
Class C
Spinal Implant
Brand: Titanium
GMP Meditech
Class C
Bone Plate
Brand: Titanium
GMP Meditech
Class C
Arthroscopy Implant
Brand: SS-Non Sterile
MJ SURGICAL
Class C
Other products from GMP Meditech
Products from the same license holder (10 products)
Bone Cutter/Punch
Brand: Maxillofacial
Class A
Spinal Cage and Cervical Disk System Instruments
Brand: Maxillofacial
Class A
Plaster Instruments and Saw
Brand: Maxillofacial
Class A
Osteotomes, Chisels & Bone Gouge
Brand: Maxillofacial
Class A
Elevators
Brand: Maxillofacial
Class A
Spinal Instruments
Brand: Maxillofacial
Class A
Cervical and Mesh System Instruments
Brand: Maxillofacial
Class A
Instruments set for Bone Screw and Plates
Brand: Maxillofacial
Class A
Retractor and Extractor
Brand: Maxillofacial
Class A
Wire Tensioner Instruments
Brand: Maxillofacial
Class A
About this record

Arthroscopy Implant is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000642_af248abf25630ef2d4a0fd6cdcab5c0d_c8bba31f9c496a60473d2f4988585fd9. This device is marketed under the brand name Titanium. The license holder is GMP Meditech, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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.