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“Stryker” Navigation NAV3i Platform - Taiwan Registration 8aad1ddb80469cec1ab3eaf906651cef

Access comprehensive regulatory information for “Stryker” Navigation NAV3i Platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8aad1ddb80469cec1ab3eaf906651cef 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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8aad1ddb80469cec1ab3eaf906651cef
Registration Details
Taiwan FDA Registration: 8aad1ddb80469cec1ab3eaf906651cef
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Device Details

“Stryker” Navigation NAV3i Platform
TW: “史賽克”手術導航系統平台
Risk Class 2
MD

Registration Details

8aad1ddb80469cec1ab3eaf906651cef

Ministry of Health Medical Device Import No. 026500

DHA05602650002

Company Information

Product Details

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

K Devices for neuroscience

K4560 Instrument for stereotaxic use in the nervous system

Imported from abroad

Dates and Status

Sep 02, 2014

Sep 02, 2024