Taiwan FDA registration 4dc19696f85a7a492b5ab1dccf654cf3
"Ames" Alibet prolapse repair system
TW: “艾梅斯”愛力倍特脫垂修補系統
Taiwan·Risk Class 2·AMS Medical Systems Ireland Limited·Registered Aug 25, 2010 – Aug 25, 2020CancelledRegistration details
- Analysis ID
- 4dc19696f85a7a492b5ab1dccf654cf3
- Customs Code
- DHA00602132900
Company information
- Manufacturer
- AMS Medical Systems Ireland Limited
- Manufacturer Country
- Ireland
- Authorized Representative
- KUANPIRE ENTERPRISES CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- import
Dates and status
- Registration Date
- Aug 25, 2010
- Expiry Date
- Aug 25, 2020
- Cancellation Date
- Sep 19, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Ames" Alibet prolapse repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dc19696f85a7a492b5ab1dccf654cf3 and manufactured by AMS Medical Systems Ireland Limited. The authorized representative in Taiwan is KUANPIRE ENTERPRISES CORPORATION.
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