Taiwan FDA registration d45c1fd4f80715a99529d08c8ce03e5b
"Tecko" Haiweijia vertebrae cement system
TW: “特科渼”海維佳脊椎骨水泥系統
Taiwan·Risk Class 2·TEKNIMED SAS;; Teknimed SAS·Registered Feb 08, 2018 – Feb 08, 2028ActiveRegistration details
- Analysis ID
- d45c1fd4f80715a99529d08c8ce03e5b
- Customs Code
- DHA05603087001
Company information
- Manufacturer
- TEKNIMED SAS;; Teknimed SAS
- Manufacturer Country
- France
- Authorized Representative
- CHEER BIOMEDICAL CORP.
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.3027 PMMA骨水泥
- Import Information
- import
Dates and status
- Registration Date
- Feb 08, 2018
- Expiry Date
- Feb 08, 2028
About this record
Access comprehensive regulatory information for "Tecko" Haiweijia vertebrae cement system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d45c1fd4f80715a99529d08c8ce03e5b and manufactured by TEKNIMED SAS;; Teknimed SAS. The authorized representative in Taiwan is CHEER BIOMEDICAL CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices