Taiwan FDA registration 0985853082da4bde6afa0999c7aacee5
“Exactech” Optecure Allograft Demineralized Bone Matrix
TW: “美精技”悠補骨補骨材料
Taiwan·Risk Class 2·MD·EXACTECH INC.·Registered Jun 02, 2015 – Jun 02, 2025ExpiredRegistration details
- Analysis ID
- 0985853082da4bde6afa0999c7aacee5
- License Form
- Ministry of Health Medical Device Import No. 027409
- Customs Code
- DHA05602740908
Company information
- Manufacturer
- EXACTECH INC.
- Manufacturer Country
- United States
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3045 Resorbed calcium salt bone cavity filling device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 02, 2015
- Expiry Date
- Jun 02, 2025
About this record
Access comprehensive regulatory information for “Exactech” Optecure Allograft Demineralized Bone Matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0985853082da4bde6afa0999c7aacee5 and manufactured by EXACTECH INC.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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