Taiwan FDA registration ba30e27ba8c6b9da359a76688059567b
“Biomet” Comprehensive Reverse Shoulder Augmented Baseplate
TW: “邦美”康臂加強墊塊底盤
Taiwan·Risk Class 2·MD·BIOMET ORTHOPEDICS·Registered Mar 30, 2021 – Mar 30, 2026ExpiredRegistration details
- Analysis ID
- ba30e27ba8c6b9da359a76688059567b
- License Form
- Ministry of Health Medical Device Import No. 034416
- Customs Code
- DHA05603441609
Company information
- Manufacturer
- BIOMET ORTHOPEDICS
- 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)
- N3660 Semi-restricted shoulder joint metal/polymer cement compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 30, 2021
- Expiry Date
- Mar 30, 2026
About this record
Access comprehensive regulatory information for “Biomet” Comprehensive Reverse Shoulder Augmented Baseplate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba30e27ba8c6b9da359a76688059567b and manufactured by BIOMET ORTHOPEDICS. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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