Taiwan FDA registration 0859b4374266a8cf2d53e5a9d04fd3c1
“Biomet” Oxford Fixed Lateral Partial Knee System
TW: “邦美”奧斯福單側人工膝關節系統
Taiwan·Risk Class 2·MD·BIOMET UK LIMITED·Registered Jan 12, 2017 – Jan 12, 2027ActiveRegistration details
- Analysis ID
- 0859b4374266a8cf2d53e5a9d04fd3c1
- License Form
- Ministry of Health Medical Device Import No. 029337
- Customs Code
- DHA05602933706
Company information
- Manufacturer
- BIOMET UK LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., 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)
- N3530 Semi-restrictive knee tibial metal/polymeric cement-type compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 12, 2017
- Expiry Date
- Jan 12, 2027
About this record
Access comprehensive regulatory information for “Biomet” Oxford Fixed Lateral Partial Knee System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0859b4374266a8cf2d53e5a9d04fd3c1 and manufactured by BIOMET UK LIMITED. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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