Taiwan FDA registration b2e376270ebc347f985847bda8a8e5df
"Zimmer" Kandy acetabular cup and bone nail
TW: “捷邁”康堤髖臼杯及骨釘
Registration details
- Analysis ID
- b2e376270ebc347f985847bda8a8e5df
- Customs Code
- DHA00602239301
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
- May 16, 2011
- Expiry Date
- May 16, 2026
About this record
Access comprehensive regulatory information for "Zimmer" Kandy acetabular cup and bone nail in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b2e376270ebc347f985847bda8a8e5df and manufactured by ZIMMER, INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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