“Teleflex Arrow” Intra-Aortic Balloon Catheters - Taiwan Registration c24a5e4dbd0b6e10d1eb2c4ba56d2cc4
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..
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Device Details
Registration Details
c24a5e4dbd0b6e10d1eb2c4ba56d2cc4
Ministry of Health Medical Device Import No. 031220
DHA05603122003
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular devices
E3535 Control system for balloon dilation and control in the aortic arch
Imported from abroad
Dates and Status
Jul 22, 2018
Jul 22, 2023

