"Stryker" arthroscopy - LeeVision series - Taiwan Registration 51fa93ae88ee95e880f021846152ed0a
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).
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 Database
Powered by Pure Global AI
89,000+ Devices
51fa93ae88ee95e880f021846152ed0a
Registration Details
Taiwan FDA Registration: 51fa93ae88ee95e880f021846152ed0a
Device Details
"Stryker" arthroscopy - LeeVision series
TW: โๅฒ่ณฝๅ
โ้็ฏ้ก-็่ฆ็ณปๅ
Risk Class 2

