Taiwan FDA registration 6f429e0510127cbed9c60a329791772d
“Zimmer” Comprehensive Reverse Shoulder System
TW: “捷邁”康品恆禧福反置式肩關節系統
Taiwan·Risk Class 2·MD·ZIMMER, INC.·Registered Nov 13, 2019 – Nov 13, 2024ExpiredRegistration details
- Analysis ID
- 6f429e0510127cbed9c60a329791772d
- License Form
- Ministry of Health Medical Device Import No. 032996
- Customs Code
- DHA05603299604
Company information
- Manufacturer
- ZIMMER, INC.
- 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
- Nov 13, 2019
- Expiry Date
- Nov 13, 2024
About this record
Access comprehensive regulatory information for “Zimmer” Comprehensive Reverse Shoulder System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6f429e0510127cbed9c60a329791772d and manufactured by ZIMMER, INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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