Taiwan FDA registration c24a5e4dbd0b6e10d1eb2c4ba56d2cc4
“Teleflex Arrow” Intra-Aortic Balloon Catheters
TW: “泰利福亞諾”主動脈球囊導管
Taiwan·Risk Class 3·MD·ARROW INTERNATIONAL INC.·Registered Jul 22, 2018 – Jul 22, 2023ExpiredRegistration details
- Analysis ID
- c24a5e4dbd0b6e10d1eb2c4ba56d2cc4
- License Form
- Ministry of Health Medical Device Import No. 031220
- Customs Code
- DHA05603122003
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 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
- Jul 22, 2018
- Expiry Date
- Jul 22, 2023
About this record
Access comprehensive regulatory information for “Teleflex Arrow” Intra-Aortic Balloon Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c24a5e4dbd0b6e10d1eb2c4ba56d2cc4 and manufactured by ARROW INTERNATIONAL INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices