"McKovei" aortic balloon catheter
Taiwan·Risk Class 3·DATASCOPE CORP.·Registered Oct 14, 2008 – Oct 14, 2028Active- Analysis ID
- 16f7800fe4d9d7b8e591bacb06586421
- Customs Code
- DHA00601927409
- Manufacturer
- DATASCOPE CORP.
- Manufacturer Country
- United States
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
- 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
- Registration Date
- Oct 14, 2008
- Expiry Date
- Oct 14, 2028
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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 3 medical device is registered under number 16f7800fe4d9d7b8e591bacb06586421 and manufactured by DATASCOPE CORP.. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DATASCOPE CORP., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.