Taiwan FDA registration ec29c8f8cb47e2d047a1d0c5efe352ea
“Biomet” A.L.P.S. Distal Tibia Plating System
TW: “邦美”阿爾卑斯系列遠端脛骨板系統
Taiwan·Risk Class 2·MD·Biomet Trauma·Registered Aug 10, 2018 – Aug 10, 2028ActiveRegistration details
- Analysis ID
- ec29c8f8cb47e2d047a1d0c5efe352ea
- License Form
- Ministry of Health Medical Device Import No. 031552
- Customs Code
- DHA05603155202
Company information
- Manufacturer
- Biomet Trauma
- Manufacturer Country
- United States
- Authorized Representative
- ZIMMER BIOMET 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)
- N3030 Single or multi-metal bone fixation device and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 10, 2018
- Expiry Date
- Aug 10, 2028
About this record
Access comprehensive regulatory information for “Biomet” A.L.P.S. Distal Tibia Plating System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec29c8f8cb47e2d047a1d0c5efe352ea and manufactured by Biomet Trauma. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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