Taiwan FDA registration 1eca794ff0207be691066aaf786be50a
"Zimmer" Messi hydroxyapatite acetabular cup system
TW: “捷邁”梅西無羥基磷灰石髖臼杯系統
Taiwan·Risk Class 3·ZIMMER GMBH·Registered Jan 18, 2011 – Jan 18, 2016CancelledRegistration details
- Analysis ID
- 1eca794ff0207be691066aaf786be50a
- Customs Code
- DHA00602190602
Company information
- Manufacturer
- ZIMMER GMBH
- Manufacturer Country
- Switzerland
- 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.3320 Semi-restrictive hip metal/metal cemented acetabular assemblies for the supplement
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2011
- Expiry Date
- Jan 18, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Zimmer" Messi hydroxyapatite acetabular cup system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1eca794ff0207be691066aaf786be50a and manufactured by ZIMMER GMBH. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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