Taiwan FDA registration 22992c1e39833eae9d0b19d4f0bae221
“Zimmer” Trilogy Acetabular System
TW: “捷邁”人工髖關節臼杯
Taiwan·Risk Class 2·MD·ZIMMER,INC.·Registered Jan 29, 2014 – Jan 29, 2029ActiveRegistration details
- Analysis ID
- 22992c1e39833eae9d0b19d4f0bae221
- License Form
- Ministry of Health Medical Device Import No. 025775
- Customs Code
- DHA05602577500
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)
- N3350 Semi-restricted hip metal/polymer cement compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 29, 2014
- Expiry Date
- Jan 29, 2029
About this record
Access comprehensive regulatory information for “Zimmer” Trilogy Acetabular System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22992c1e39833eae9d0b19d4f0bae221 and manufactured by ZIMMER,INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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