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"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).

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51fa93ae88ee95e880f021846152ed0a
Registration Details
Taiwan FDA Registration: 51fa93ae88ee95e880f021846152ed0a
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Device Details

"Stryker" arthroscopy - LeeVision series
TW: โ€œๅฒ่ณฝๅ…‹โ€้—œ็ฏ€้ก-็†่ฆ–็ณปๅˆ—
Risk Class 2

Registration Details

51fa93ae88ee95e880f021846152ed0a

DHA00602239900

Company Information

United States;;Germany

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.1100 Closing Lenses

Input;; Contract manufacturing

Dates and Status

May 16, 2011

May 16, 2026