Taiwan FDA registration 1ab104e6c18367b09679d58badeee80b
“Stryker” Cascadia AN 3D Interbody System
TW: “史賽克”凱思卡迪亞三維椎體系統
Taiwan·Risk Class 2·MD·K2M, INC.·Registered Apr 20, 2022 – Apr 20, 2027ActiveRegistration details
- Analysis ID
- 1ab104e6c18367b09679d58badeee80b
- License Form
- Ministry of Health Medical Device Import No. 035394
- Customs Code
- DHA05603539404
Company information
- Manufacturer
- K2M, INC.
- 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)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 20, 2022
- Expiry Date
- Apr 20, 2027
About this record
Access comprehensive regulatory information for “Stryker” Cascadia AN 3D Interbody System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ab104e6c18367b09679d58badeee80b and manufactured by K2M, INC.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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