Taiwan FDA registration 5b639add5e135dff183c26c1784ff904
"Zimmer" bone metal artificial shoulder glenoid
TW: “捷邁”骨金屬人工肩盂
Taiwan·Risk Class 2·ZIMMER TRABECULAR METAL TECHNOLOGY, INC.·Registered Feb 17, 2012 – Feb 17, 2017CancelledRegistration details
- Analysis ID
- 5b639add5e135dff183c26c1784ff904
- Customs Code
- DHA00602326000
Company information
- Manufacturer
- ZIMMER TRABECULAR METAL TECHNOLOGY, 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 Orthopedics
- Product Type (Level 2)
- N.3660 Semi-restrictive shoulder jointsMetallic/polymer-like bone cement supplements
- Import Information
- import
Dates and status
- Registration Date
- Feb 17, 2012
- Expiry Date
- Feb 17, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Zimmer" bone metal artificial shoulder glenoid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5b639add5e135dff183c26c1784ff904 and manufactured by ZIMMER TRABECULAR METAL TECHNOLOGY, INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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