Taiwan FDA registration 12d04009badfd7658698820d97ea628c
McKovei aortic balloon catheter
TW: 邁柯唯主動脈球囊導管
Taiwan·Risk Class 2·DATASCOPE CORP.·Registered Dec 22, 2011 – Dec 22, 2021CancelledRegistration details
- Analysis ID
- 12d04009badfd7658698820d97ea628c
- Customs Code
- DHA00602317305
Company information
- Manufacturer
- DATASCOPE CORP.
- 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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3535 Intraarchary Aortic Balloon Dilation and Control System
- Import Information
- import
Dates and status
- Registration Date
- Dec 22, 2011
- Expiry Date
- Dec 22, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for McKovei aortic balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12d04009badfd7658698820d97ea628c and manufactured by DATASCOPE CORP.. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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