Taiwan FDA registration f1a31aa59095529c74742265988c399d
“Stryker” CASCADIA Cervical 3D Interbody System
TW: “史賽克”凱思卡迪亞頸椎椎體系統
Taiwan·Risk Class 2·MD·K2M, INC.·Registered Jul 11, 2022 – Jul 11, 2027ActiveRegistration details
- Analysis ID
- f1a31aa59095529c74742265988c399d
- License Form
- Ministry of Health Medical Device Import No. 035705
- Customs Code
- DHA05603570508
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
- Jul 11, 2022
- Expiry Date
- Jul 11, 2027
About this record
Access comprehensive regulatory information for “Stryker” CASCADIA Cervical 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 f1a31aa59095529c74742265988c399d and manufactured by K2M, INC.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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