Taiwan FDA registration ec5da38766204d9c264178fddb056bde
"Ames" light mesh prolapse repair system
TW: “艾梅斯”阿博奇輕網脫垂修補系統
Taiwan·Risk Class 2·AMS Medical Systems Ireland Limited·Registered Sep 08, 2008 – Sep 08, 2018CancelledRegistration details
- Analysis ID
- ec5da38766204d9c264178fddb056bde
- Customs Code
- DHA00601920401
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
- Sep 08, 2008
- Expiry Date
- Sep 08, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ames" light mesh 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 ec5da38766204d9c264178fddb056bde and manufactured by AMS Medical Systems Ireland Limited. The authorized representative in Taiwan is KUANPIRE ENTERPRISES CORPORATION.
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