Taiwan FDA registration 3f93fff7211ac30f02a1a92dd68e1fcb
“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
Taiwan·Risk Class 2·MD·ZIMMER TRABECULAR METAL TECHNOLOGY, INC.·Registered Mar 15, 2016 – Mar 15, 2026ExpiredRegistration details
- Analysis ID
- 3f93fff7211ac30f02a1a92dd68e1fcb
- License Form
- Ministry of Health Medical Device Import No. 028228
- Customs Code
- DHA05602822809
Company information
- Manufacturer
- ZIMMER TRABECULAR METAL TECHNOLOGY, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ZimVie Taiwan Co., Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 15, 2016
- Expiry Date
- Mar 15, 2026
About this record
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..
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