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“Medtronic ” POWEREASE System Working Ends - Taiwan Registration c303c0a9934a9bbc1539fd878c9ebabb

Access comprehensive regulatory information for “Medtronic ” POWEREASE System Working Ends in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c303c0a9934a9bbc1539fd878c9ebabb and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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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c303c0a9934a9bbc1539fd878c9ebabb
Registration Details
Taiwan FDA Registration: c303c0a9934a9bbc1539fd878c9ebabb
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Device Details

“Medtronic ” POWEREASE System Working Ends
TW: “美敦力”動力系統器械
Risk Class 2
MD

Registration Details

c303c0a9934a9bbc1539fd878c9ebabb

Ministry of Health Medical Device Import No. 031572

DHA05603157208

Company Information

United States

Product Details

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

K Devices for neuroscience

K4310 Power Simple Head Cap, File, Ring Saw and Its Accessories

Imported from abroad

Dates and Status

Aug 28, 2018

Aug 28, 2028