Taiwan FDA registration 4197a346dcb7022357e4c8da3d101e0c
"Zimmer" Fijian lumbar intervertebral fusion device
TW: ＂捷邁＂斐濟腰椎椎間融合器
Taiwan·Risk Class 2·ZIMMER SPINE·Registered Jun 23, 2006 – Jun 23, 2026ExpiredRegistration details
- Analysis ID
- 4197a346dcb7022357e4c8da3d101e0c
- Customs Code
- DHA00601673201
Company information
- Manufacturer
- ZIMMER SPINE
- Manufacturer Country
- France
- 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
- Import Information
- import
Dates and status
- Registration Date
- Jun 23, 2006
- Expiry Date
- Jun 23, 2026
About this record
Access comprehensive regulatory information for "Zimmer" Fijian lumbar 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 4197a346dcb7022357e4c8da3d101e0c and manufactured by ZIMMER SPINE. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..
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