Taiwan FDA registration d4cb8522308050bda7155152011d876d
“Biomet” Oxford 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 Jul 10, 2017 – Jul 10, 2027ActiveRegistration details
- Analysis ID
- d4cb8522308050bda7155152011d876d
- License Form
- Ministry of Health Medical Device Import No. 029939
- Customs Code
- DHA05602993908
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
- Jul 10, 2017
- Expiry Date
- Jul 10, 2027
About this record
Access comprehensive regulatory information for “Biomet” Oxford 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 d4cb8522308050bda7155152011d876d and manufactured by BIOMET UK LIMITED. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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