Taiwan FDA registration 51fa93ae88ee95e880f021846152ed0a
"Stryker" arthroscopy - LeeVision series
TW: “史賽克”關節鏡-理視系列
Taiwan·Risk Class 2·HENKE-SASS, WOLF GMBH;; STRYKER ENDOSCOPY·Registered May 16, 2011 – May 16, 2026ExpiredRegistration details
- Analysis ID
- 51fa93ae88ee95e880f021846152ed0a
- Customs Code
- DHA00602239900
Company information
- Manufacturer
- HENKE-SASS, WOLF GMBH;; STRYKER ENDOSCOPY
- Manufacturer Country
- United States;;Germany
- 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 Orthopedics
- Product Type (Level 2)
- N.1100 Closing Lenses
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- May 16, 2011
- Expiry Date
- May 16, 2026
About this record
Access comprehensive regulatory information for "Stryker" arthroscopy - LeeVision series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51fa93ae88ee95e880f021846152ed0a and manufactured by HENKE-SASS, WOLF GMBH;; STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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