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"Stryker" precision HD arthroscopy - Taiwan Registration 71f36e0dfa0988d0e6d0061f9059f934

Access comprehensive regulatory information for "Stryker" precision HD arthroscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71f36e0dfa0988d0e6d0061f9059f934 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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71f36e0dfa0988d0e6d0061f9059f934
Registration Details
Taiwan FDA Registration: 71f36e0dfa0988d0e6d0061f9059f934
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Device Details

"Stryker" precision HD arthroscopy
TW: โ€œๅฒ่ณฝๅ…‹โ€็ฒพๆบ–้ซ˜ๆธ…้—œ็ฏ€้ก
Risk Class 2

Registration Details

71f36e0dfa0988d0e6d0061f9059f934

DHA05603336207

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

Mar 01, 2020

Mar 01, 2030