Taiwan FDA registration bb4705fd7256e5a7758fd17d536d7634
"Tekme" He-Man artificial replacement bone
TW: “泰克美” 希曼骼人工替代骨
Taiwan·Risk Class 2·TEKNIMED SAS·Registered Oct 28, 2010 – Oct 28, 2015CancelledRegistration details
- Analysis ID
- bb4705fd7256e5a7758fd17d536d7634
- Customs Code
- DHA00602160600
Company information
- Manufacturer
- TEKNIMED SAS
- Manufacturer Country
- France
- Authorized Representative
- GREAT UNITED STRONG ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3045 Absorbable Calcium Salt Bone Cavity Filling Device
- Import Information
- import
Dates and status
- Registration Date
- Oct 28, 2010
- Expiry Date
- Oct 28, 2015
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Tekme" He-Man artificial replacement bone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bb4705fd7256e5a7758fd17d536d7634 and manufactured by TEKNIMED SAS. The authorized representative in Taiwan is GREAT UNITED STRONG ENTERPRISE CO., LTD..
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