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“Zimmer” NavitrackER Reference Marker Device - Taiwan Registration 09cb1e54d721f900384cf424d634c499

Access comprehensive regulatory information for “Zimmer” NavitrackER Reference Marker Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09cb1e54d721f900384cf424d634c499 and manufactured by ZIMMER CAS. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..

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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09cb1e54d721f900384cf424d634c499
Registration Details
Taiwan FDA Registration: 09cb1e54d721f900384cf424d634c499
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Device Details

“Zimmer” NavitrackER Reference Marker Device
TW: “捷邁”導航標記裝置
Risk Class 2
MD

Registration Details

09cb1e54d721f900384cf424d634c499

Ministry of Health Medical Device Import No. 034576

DHA05603457605

Company Information

Canada

Product Details

Details are as detailed as approved Chinese instructions

K Devices for neuroscience

K4560 Instrument for stereotaxic use in the nervous system

Imported from abroad

Dates and Status

May 28, 2021

May 28, 2026