Taiwan FDA registration 4cb58b5055efb2076ff9e56c9c47bf17
"Zimmer" Tri Eti acetabular cup system
TW: “捷邁”崔勒艾提髖臼杯系統
Taiwan·Risk Class 2·ZIMMER, INC.·Registered Dec 13, 2010 – Dec 13, 2025ExpiredRegistration details
- Analysis ID
- 4cb58b5055efb2076ff9e56c9c47bf17
- Customs Code
- DHA00602183502
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 Orthopedics
- Product Type (Level 2)
- N.3358 Semi-restricted correlated metals/polymers/metals porous coating and cementless cement supplements
- Import Information
- import
Dates and status
- Registration Date
- Dec 13, 2010
- Expiry Date
- Dec 13, 2025
About this record
Access comprehensive regulatory information for "Zimmer" Tri Eti acetabular cup system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4cb58b5055efb2076ff9e56c9c47bf17 and manufactured by ZIMMER, INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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