“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.
Device Details
Registration Details
3f93fff7211ac30f02a1a92dd68e1fcb
Ministry of Health Medical Device Import No. 028228
DHA05602822809
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

