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"Zimmer" cervical intervertebral fusion device - Taiwan Registration 8f0da69b6c2fd3dd533f8213d10de35c

Access comprehensive regulatory information for "Zimmer" cervical intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f0da69b6c2fd3dd533f8213d10de35c and manufactured by ZIMMER SPINE. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ZIMMER SPINE, and 1 recent registrations in the same category. 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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8f0da69b6c2fd3dd533f8213d10de35c
Registration Details
Taiwan FDA Registration: 8f0da69b6c2fd3dd533f8213d10de35c
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Device Details

"Zimmer" cervical intervertebral fusion device
TW: "ๆท้‚" ้ ธๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2

Registration Details

8f0da69b6c2fd3dd533f8213d10de35c

DHA00601108403

Company Information

France

Product Details

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

N Orthopedics

import

Dates and Status

Mar 08, 2005

Mar 08, 2025

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