Taiwan FDA registration 540ba54bf750d04f1bbd5780f0e32866
"Bangmei" funnel chest correction system
TW: “邦美”漏斗胸矯正系統
Taiwan·Risk Class 2·BIOMET MICROFIXATION ;; BIOMET INC.·Registered May 21, 2021 – May 21, 2026ExpiredRegistration details
- Analysis ID
- 540ba54bf750d04f1bbd5780f0e32866
- Customs Code
- DHA05603456003
Company information
- Manufacturer
- BIOMET MICROFIXATION ;; BIOMET INC.
- Manufacturer Country
- United States
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- May 21, 2021
- Expiry Date
- May 21, 2026
About this record
Access comprehensive regulatory information for "Bangmei" funnel chest correction system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 540ba54bf750d04f1bbd5780f0e32866 and manufactured by BIOMET MICROFIXATION ;; BIOMET INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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