Taiwan FDA registration e4ba0a38847b42ab73aad110aad518bf

"Stryker" arthroscopic hand tools (unsterilized)

TW: "史賽克" 關節鏡手動工具(未滅菌)

Taiwan·Risk Class 1·HENKE-SASS, WOLF GMBH;; STRYKER ENDOSCOPY·Registered Nov 06, 2020 – Nov 06, 2025Expired

Registration details

Analysis ID: e4ba0a38847b42ab73aad110aad518bf
Customs Code: DHA09402208901

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: Limited to the first level identification range of the classification and grading management method for medical equipment "Arthroscopy (N.1100)".
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.1100 Closing Lenses
Import Information: Input;; Contract manufacturing

Dates and status

Registration Date: Nov 06, 2020
Expiry Date: Nov 06, 2025

About this record

Access comprehensive regulatory information for "Stryker" arthroscopic hand tools (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e4ba0a38847b42ab73aad110aad518bf and manufactured by HENKE-SASS, WOLF GMBH;; STRYKER ENDOSCOPY. 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.