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“Stryker” Navigation Kit for NavSuite - Taiwan Registration 1f8badf4fdd96be1736f1c8ac550dbdb

Access comprehensive regulatory information for “Stryker” Navigation Kit for NavSuite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1f8badf4fdd96be1736f1c8ac550dbdb and manufactured by 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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1f8badf4fdd96be1736f1c8ac550dbdb
Registration Details
Taiwan FDA Registration: 1f8badf4fdd96be1736f1c8ac550dbdb
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Device Details

“Stryker” Navigation Kit for NavSuite
TW: “史賽克”導航手術室專用套件
Risk Class 2
MD
Cancelled

Registration Details

1f8badf4fdd96be1736f1c8ac550dbdb

Ministry of Health Medical Device Import No. 026168

DHA05602616807

Company Information

Product Details

K Devices for neuroscience

K4560 Instrument for stereotaxic use in the nervous system

Imported from abroad

Dates and Status

May 15, 2014

May 15, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者