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"Stryker" third generation titanium alloy locking bone plate system - Taiwan Registration 9e5d7be49050bbef95aacddb45a37e39

Access comprehensive regulatory information for "Stryker" third generation titanium alloy locking bone 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 9e5d7be49050bbef95aacddb45a37e39 and manufactured by Stryker GmbH. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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9e5d7be49050bbef95aacddb45a37e39
Registration Details
Taiwan FDA Registration: 9e5d7be49050bbef95aacddb45a37e39
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Device Details

"Stryker" third generation titanium alloy locking bone plate system
TW: โ€œๅฒ่ณฝๅ…‹โ€็ฌฌไธ‰ไปฃ้ˆฆๅˆ้‡‘้Ž–ๅฎš้ชจๆฟ็ณป็ตฑ
Risk Class 2

Registration Details

9e5d7be49050bbef95aacddb45a37e39

DHA05602872905

Company Information

Switzerland

Product Details

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

N Orthopedics

N.3030 Single or multiple metallic bone fixation devices and accessories

import

Dates and Status

Aug 12, 2016

Aug 12, 2026