Taiwan FDA registration 2b38f010ba484070d9cde95ae8a0d3d1
"Holmedeka-Osterning" 7000 series full artificial knee joint system
TW: “好美得卡-奧斯得寧”7000系列全人工膝關節系統
Taiwan·Risk Class 2·HOWMEDICA OSTEONICS CORP.·Registered Nov 09, 2010 – Nov 09, 2025ExpiredRegistration details
- Analysis ID
- 2b38f010ba484070d9cde95ae8a0d3d1
- Customs Code
- DHA00602165500
Company information
- Manufacturer
- HOWMEDICA OSTEONICS CORP.
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
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.3560 Semi-restrictive knee joints of the femoral bone polymers/metallics/polymers
- Import Information
- import
Dates and status
- Registration Date
- Nov 09, 2010
- Expiry Date
- Nov 09, 2025
About this record
Access comprehensive regulatory information for "Holmedeka-Osterning" 7000 series full artificial knee joint system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b38f010ba484070d9cde95ae8a0d3d1 and manufactured by HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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