Taiwan FDA registration 94ab9c5b5e33469e6cfc7ea9c5ea17c0
“TEKNIMED” NANOGEL Synthetic Bone Substitute
TW: “泰克美”耐優捷凝膠人工骨泥
Taiwan·Risk Class 2·MD·Teknimed SAS·Registered Jun 10, 2022 – Jun 10, 2027ActiveRegistration details
- Analysis ID
- 94ab9c5b5e33469e6cfc7ea9c5ea17c0
- License Form
- Ministry of Health Medical Device Import No. 035578
- Customs Code
- DHA05603557801
Company information
- Manufacturer
- Teknimed SAS
- Manufacturer Country
- France
- Authorized Representative
- GREAT UNITED STRONG ENTERPRISE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3045 Absorbable calcium salt bone cavity filling device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 10, 2022
- Expiry Date
- Jun 10, 2027
About this record
Access comprehensive regulatory information for “TEKNIMED” NANOGEL Synthetic Bone Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94ab9c5b5e33469e6cfc7ea9c5ea17c0 and manufactured by Teknimed SAS. The authorized representative in Taiwan is GREAT UNITED STRONG ENTERPRISE CO., LTD..
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