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Stryker Manual Orthopedic Instruments (Sterilization) - Taiwan Registration f7daf8b957443e410c4a71eabdd55c43

Access comprehensive regulatory information for Stryker Manual Orthopedic Instruments (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7daf8b957443e410c4a71eabdd55c43 and manufactured by STRYKER TRAUMA GMBH.. 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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f7daf8b957443e410c4a71eabdd55c43
Registration Details
Taiwan FDA Registration: f7daf8b957443e410c4a71eabdd55c43
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Device Details

Stryker Manual Orthopedic Instruments (Sterilization)
TW: โ€œๅฒ่ณฝๅ…‹โ€ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f7daf8b957443e410c4a71eabdd55c43

DHA04400709207

Company Information

Germany

Product Details

Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.

N Orthopedics

N.4540 ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Sep 24, 2008

Sep 24, 2018

Aug 05, 2022

Cancellation Information

Logged out

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