Taiwan FDA registration 0109ade5a956c9e23a8810075b3727de
"Arno" intra-aortic balloon pump
TW: “亞諾”主動脈內氣球幫浦
Taiwan·Risk Class 3·ARROW INTERNATIONAL INC.·Registered Oct 29, 2010 – Oct 29, 2025ExpiredRegistration details
- Analysis ID
- 0109ade5a956c9e23a8810075b3727de
- Customs Code
- DHA00602161004
Company information
- Manufacturer
- ARROW INTERNATIONAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN 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
- Oct 29, 2010
- Expiry Date
- Oct 29, 2025
About this record
Access comprehensive regulatory information for "Arno" 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 0109ade5a956c9e23a8810075b3727de and manufactured by ARROW INTERNATIONAL INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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