Taiwan FDA registration c6e7866a5595f754b5dbca107a9e9a2e
“Stryker” AIR+ All-Inside Meniscal Repair System
TW: “史賽克”艾爾半月板修復系統
Taiwan·Risk Class 2·MD·STRYKER ENDOSCOPY·Registered Nov 29, 2021 – Nov 29, 2026ActiveRegistration details
- Analysis ID
- c6e7866a5595f754b5dbca107a9e9a2e
- License Form
- Ministry of Health Medical Device Import No. 035071
- Customs Code
- DHA05603507106
Company information
- Manufacturer
- STRYKER ENDOSCOPY
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 29, 2021
- Expiry Date
- Nov 29, 2026
About this record
Access comprehensive regulatory information for “Stryker” AIR+ All-Inside Meniscal Repair System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6e7866a5595f754b5dbca107a9e9a2e and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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