Taiwan FDA registration 5ebaec3edfd27d49601f35464fedeaf2
"Ames" Alibet Parcy type prolapse repair system
TW: “艾梅斯”愛力倍特帕西型脫垂修補系統
Taiwan·Risk Class 2·AMERICAN MEDICAL SYSTEMS·Registered Mar 22, 2013 – Mar 22, 2018CancelledRegistration details
- Analysis ID
- 5ebaec3edfd27d49601f35464fedeaf2
- Customs Code
- DHA00602479709
Company information
- Manufacturer
- AMERICAN MEDICAL SYSTEMS
- Manufacturer Country
- United States
- 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
- Mar 22, 2013
- Expiry Date
- Mar 22, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ames" Alibet Parcy type 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 5ebaec3edfd27d49601f35464fedeaf2 and manufactured by AMERICAN MEDICAL SYSTEMS. The authorized representative in Taiwan is KUANPIRE ENTERPRISES CORPORATION.
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