Taiwan FDA registration da4301fe6215c58ceab1d09e0947859f
"Artreen" Pleg polypropylene mesh
TW: “亞翠恩”普來聚丙烯網片
Taiwan·Risk Class 2·ATRIUM MEDICAL CORPORATION·Registered Sep 17, 2008 – Sep 17, 2018CancelledRegistration details
- Analysis ID
- da4301fe6215c58ceab1d09e0947859f
- Customs Code
- DHA00601921901
Company information
- Manufacturer
- ATRIUM MEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
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
- Import Information
- import
Dates and status
- Registration Date
- Sep 17, 2008
- Expiry Date
- Sep 17, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Artreen" Pleg polypropylene mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number da4301fe6215c58ceab1d09e0947859f and manufactured by ATRIUM MEDICAL CORPORATION. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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