Taiwan FDA registration 8af24486b120b27cbee22908aa15a0cc
“Synthes” VA-LCP Condylar Plate
TW: “信迪思”多角度鎖定加壓股骨髁骨板
Taiwan·Risk Class 2·MD·SYNTHES GMBH·Registered Oct 12, 2017 – Oct 12, 2027ActiveRegistration details
- Analysis ID
- 8af24486b120b27cbee22908aa15a0cc
- License Form
- Ministry of Health Medical Device Import No. 030337
- Customs Code
- DHA05603033706
Company information
- Manufacturer
- SYNTHES GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
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)
- N3030 Single or multi-metal bone fixation device and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 12, 2017
- Expiry Date
- Oct 12, 2027
About this record
Access comprehensive regulatory information for “Synthes” VA-LCP Condylar Plate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8af24486b120b27cbee22908aa15a0cc and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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