Taiwan FDA registration 2b5cf5edfa0fcdc223c5bc0626eb5af4
“Stryker” OMEGA PEEK Knotless Anchor System
TW: “史賽克”無結錨釘固定系統
Taiwan·Risk Class 2·MD·STRYKER ENDOSCOPY·Registered Nov 05, 2020 – Nov 05, 2025ExpiredRegistration details
- Analysis ID
- 2b5cf5edfa0fcdc223c5bc0626eb5af4
- License Form
- Ministry of Health Medical Device Import No. 034016
- Customs Code
- DHA05603401606
Company information
- Manufacturer
- STRYKER ENDOSCOPY
- 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 Orthopedic devices
- Product Type (Level 2)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 05, 2020
- Expiry Date
- Nov 05, 2025
About this record
Access comprehensive regulatory information for “Stryker” OMEGA PEEK Knotless Anchor System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b5cf5edfa0fcdc223c5bc0626eb5af4 and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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