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"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).

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.

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234a2ef29175e6c451505c368f73b3e6
Registration Details
Taiwan FDA Registration: 234a2ef29175e6c451505c368f73b3e6
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Device Details

"Stryker" Profio titanium hand and ossicle plate system
TW: "ๅฒ่ณฝๅ…‹" ๆ™ฎ็พ…่ฒๆญ้ˆฆ่ณชๆ‰‹้ƒจ่ˆ‡ๅฐ้ชจๆฎต้ชจๆฟ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

234a2ef29175e6c451505c368f73b3e6

DHA00600948006

Company Information

Product Details

N000 Orthopedics

import

Dates and Status

Aug 16, 2000

Aug 16, 2025

May 04, 2022

Cancellation Information

Logged out

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