Maxillofacial Implant
- UID
- MFG/MD/2022/000642_c2636c2218692f7ce80f69e32469c14c_355d55bcce74bc1c81109502a46d4a18
- Device class
- Class C
- Brand name
- Titanium
- License holder
- GMP Meditech
- 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
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.
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