Taiwan FDA registration 3ca4978eb74131f9e3404de88a9222b3
“Biomet” A.L.P.S. Hand Fracture System
TW: “邦美”阿爾卑斯系列手部骨板系統
Taiwan·Risk Class 2·MD·Biomet Trauma·Registered Jun 23, 2017 – Jun 23, 2027ActiveRegistration details
- Analysis ID
- 3ca4978eb74131f9e3404de88a9222b3
- License Form
- Ministry of Health Medical Device Import No. 029912
- Customs Code
- DHA05602991201
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
- Jun 23, 2017
- Expiry Date
- Jun 23, 2027
About this record
Access comprehensive regulatory information for “Biomet” A.L.P.S. Hand Fracture System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ca4978eb74131f9e3404de88a9222b3 and manufactured by Biomet Trauma. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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