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“Zimmer-TMT” TM Ardis Interbody System Solid - Taiwan Registration 3f93fff7211ac30f02a1a92dd68e1fcb

Access comprehensive regulatory information for “Zimmer-TMT” TM Ardis Interbody System Solid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f93fff7211ac30f02a1a92dd68e1fcb and manufactured by ZIMMER TRABECULAR METAL TECHNOLOGY, INC.. 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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3f93fff7211ac30f02a1a92dd68e1fcb
Registration Details
Taiwan FDA Registration: 3f93fff7211ac30f02a1a92dd68e1fcb
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Device Details

“Zimmer-TMT” TM Ardis Interbody System Solid
TW: “捷邁”多孔鉭金屬亞帝斯實心椎間融合系統
Risk Class 2
MD

Registration Details

3f93fff7211ac30f02a1a92dd68e1fcb

Ministry of Health Medical Device Import No. 028228

DHA05602822809

Company Information

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Mar 15, 2016

Mar 15, 2026