Taiwan FDA registration 65215616b2ae61f75893162bd06d9498
The Stryker 7000 series is a fully artificial knee system
TW: "史賽克" 7000系列全人工膝關節系統
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered Mar 08, 2004 – Mar 08, 2024ExpiredRegistration details
- Analysis ID
- 65215616b2ae61f75893162bd06d9498
- Customs Code
- DHA00601056807
Company information
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2004
- Expiry Date
- Mar 08, 2024
- Cancellation Date
- May 07, 2024
About this record
Access comprehensive regulatory information for The Stryker 7000 series is a fully artificial 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 65215616b2ae61f75893162bd06d9498 and manufactured by STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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