Taiwan FDA registration 7bf83dcc72002d88a43a4b9acf19bbcf
"Atrien" vascular tunneler (unsterilized)
TW: “亞翠恩”血管隧道器 (未滅菌)
Taiwan·Risk Class 1·ATRIUM MEDICAL CORPORATION·Registered Oct 31, 2008 – Oct 31, 2018CancelledRegistration details
- Analysis ID
- 7bf83dcc72002d88a43a4b9acf19bbcf
- Customs Code
- DHA04400719902
Company information
- Manufacturer
- ATRIUM MEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- import
Dates and status
- Registration Date
- Oct 31, 2008
- Expiry Date
- Oct 31, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Atrien" vascular tunneler (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7bf83dcc72002d88a43a4b9acf19bbcf and manufactured by ATRIUM MEDICAL CORPORATION. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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