Taiwan FDA registration 3924589d7a721b329a34494a841cb6cf
"Zimmer" porous tantalum metal Addis intervertebral fusion system
TW: “捷邁”多孔鉭金屬亞帝斯椎間融合系統
Taiwan·Risk Class 2·ZIMMER TRABECULAR METAL TECHNOLOGY, INC.·Registered Jan 25, 2013 – Jan 25, 2028ActiveRegistration details
- Analysis ID
- 3924589d7a721b329a34494a841cb6cf
- Customs Code
- DHA00602462404
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 Orthopedics
- Product Type (Level 2)
- N.3060 椎體間之脊椎矯正固定物
- Import Information
- import
Dates and status
- Registration Date
- Jan 25, 2013
- Expiry Date
- Jan 25, 2028
About this record
Access comprehensive regulatory information for "Zimmer" porous tantalum metal Addis intervertebral fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3924589d7a721b329a34494a841cb6cf and manufactured by ZIMMER TRABECULAR METAL TECHNOLOGY, INC.. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..
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