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“Zimmer” Universal Clamp - Taiwan Registration 159645fed3b5b5ea76bc074bc29dfe93

Access comprehensive regulatory information for “Zimmer” Universal Clamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 159645fed3b5b5ea76bc074bc29dfe93 and manufactured by ZIMMER GMBH. The authorized representative in Taiwan is ZimVie 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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159645fed3b5b5ea76bc074bc29dfe93
Registration Details
Taiwan FDA Registration: 159645fed3b5b5ea76bc074bc29dfe93
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Device Details

“Zimmer” Universal Clamp
TW: “捷邁”脊椎固定裝置
Risk Class 2
MD

Registration Details

159645fed3b5b5ea76bc074bc29dfe93

Ministry of Health Medical Device Import No. 031166

DHA05603116600

Company Information

Switzerland

Product Details

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

N Orthopedic devices

N3010 Bone Fixation Ring

Imported from abroad

Dates and Status

Jun 04, 2018

Jun 04, 2023