"Stryker" Profio titanium hand and ossicle plate system - Taiwan Registration 234a2ef29175e6c451505c368f73b3e6
Access comprehensive regulatory information for "Stryker" Profio titanium hand and ossicle plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 234a2ef29175e6c451505c368f73b3e6 and manufactured by Stryker GmbH;; STRYKER LEIBINGER GMBH & CO. KG. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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234a2ef29175e6c451505c368f73b3e6
Registration Details
Taiwan FDA Registration: 234a2ef29175e6c451505c368f73b3e6
Device Details
"Stryker" Profio titanium hand and ossicle plate system
TW: "ๅฒ่ณฝๅ
" ๆฎ็พ
่ฒๆญ้ฆ่ณชๆ้จ่ๅฐ้ชจๆฎต้ชจๆฟ็ณป็ตฑ
Risk Class 2
Cancelled

