Taiwan FDA registration b53b2691c601d2201017188c7d02186c
“Datascope” Cardiosave Intra-Aortic Balloon Pump
TW: “德塔斯”主動脈氣球導管幫浦
Taiwan·Risk Class 3·MD·DATASCOPE CORPORATION·Registered Nov 07, 2013 – Nov 07, 2023ExpiredRegistration details
- Analysis ID
- b53b2691c601d2201017188c7d02186c
- License Form
- Ministry of Health Medical Device Import No. 025453
- Customs Code
- DHA05602545301
Company information
- Manufacturer
- DATASCOPE 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)
- E Cardiovascular devices
- Product Type (Level 2)
- E3535 Control system for balloon dilation and control in the aortic arch
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 07, 2013
- Expiry Date
- Nov 07, 2023
About this record
Access comprehensive regulatory information for “Datascope” Cardiosave Intra-Aortic Balloon Pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b53b2691c601d2201017188c7d02186c and manufactured by DATASCOPE CORPORATION. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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