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Stryker Image Guide Assist Accessory - Hip Module - Taiwan Registration 57e3c48fbd89b6c9fc438ff6459b07a7

Access comprehensive regulatory information for Stryker Image Guide Assist Accessory - Hip Module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57e3c48fbd89b6c9fc438ff6459b07a7 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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57e3c48fbd89b6c9fc438ff6459b07a7
Registration Details
Taiwan FDA Registration: 57e3c48fbd89b6c9fc438ff6459b07a7
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Device Details

Stryker Image Guide Assist Accessory - Hip Module
TW: "ๅฒ่ณฝๅ…‹"ๅฝฑๅƒๅฐŽๅผ•่ผ”ๅŠฉ็ณป็ตฑ้™„ไปถ-้ซ–ๆจก็ต„
Risk Class 2
Cancelled

Registration Details

57e3c48fbd89b6c9fc438ff6459b07a7

DHA00601774502

Company Information

Product Details

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

K Neuroscience

K.4560 Instruments for stereotaxic use of the nervous system

import

Dates and Status

Jan 31, 2007

Jan 31, 2017

Dec 20, 2019

Cancellation Information

Logged out

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