Maxillofacial Implant - India CDSCO Medical Device Registration

Maxillofacial Implant is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000642_c2636c2218692f7ce80f69e32469c14c_355d55bcce74bc1c81109502a46d4a18. 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.

Free Database

CDSCO Registered

Class Class C

Maxillofacial Implant

UID: MFG/MD/2022/000642_c2636c2218692f7ce80f69e32469c14c_355d55bcce74bc1c81109502a46d4a18

Brand Name

Titanium

License Holder

GMP Meditech

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Maxillofacial implant is indicated for use in fracture fixation, mandibular reconstruction and surgery involving osteotomies, orthognathic reconstruction or surgery, surgery related to dento-facial or facial cavity and trauma due to it. The intended use of these implants is to draw two or more aligned bone fragments together to facilitate healing

Class C

Nails

Brand: Titanium

Universal Orthosystems

Class C

Brand: Maxillofacial

Class A