Taiwan FDA registration d5762c0b15468a785717bf22779fe35d
“Stryker” Cascadia TL 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 Feb 25, 2022 – Feb 25, 2027ActiveRegistration details
- Analysis ID
- d5762c0b15468a785717bf22779fe35d
- License Form
- Ministry of Health Medical Device Import No. 035275
- Customs Code
- DHA05603527509
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
- Feb 25, 2022
- Expiry Date
- Feb 25, 2027
About this record
Access comprehensive regulatory information for “Stryker” Cascadia TL 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 d5762c0b15468a785717bf22779fe35d and manufactured by K2M, INC.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices