Taiwan FDA registration c0c8a85cc7500ecaa0b2ff167241df81
"Stryker" artificial tibial inner pad system
TW: "史賽克"人工脛骨內墊系統
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered Aug 10, 2006 – Aug 10, 2026ActiveRegistration details
- Analysis ID
- c0c8a85cc7500ecaa0b2ff167241df81
- Customs Code
- DHA00601698300
Company information
- Manufacturer Country
- Ireland;;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
- Aug 10, 2006
- Expiry Date
- Aug 10, 2026
About this record
Access comprehensive regulatory information for "Stryker" artificial tibial inner pad system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c0c8a85cc7500ecaa0b2ff167241df81 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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