Taiwan FDA registration 5effdfff96cff120b0cf97c58a3a035c
"Stryker" clinical model
TW: "史賽克" 臨床用樣板
Taiwan·Risk Class 1·STRYKER IRELAND LIMITED·Registered Jan 04, 2006 – Jan 04, 2011CancelledRegistration details
- Analysis ID
- 5effdfff96cff120b0cf97c58a3a035c
- Customs Code
- DHA04400245801
Company information
- Manufacturer
- STRYKER IRELAND LIMITED
- Manufacturer Country
- Ireland
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Clinical templates consist of medical molds or probes that are used to select and configure implants for surgical plastic surgery or as guidelines before cutting tissue.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4800 Sample plate for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Jan 04, 2006
- Expiry Date
- Jan 04, 2011
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Stryker" clinical model in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5effdfff96cff120b0cf97c58a3a035c and manufactured by STRYKER IRELAND LIMITED. 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