“Fuji” AP-GRIPFLOW Circulation Perfusion Catheter - Taiwan Registration 012bc31932153d59e7edbe307004d8a4
Access comprehensive regulatory information for “Fuji” AP-GRIPFLOW Circulation Perfusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 012bc31932153d59e7edbe307004d8a4 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is YOO-HOO Limited.
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Device Details
Registration Details
012bc31932153d59e7edbe307004d8a4
Ministry of Health Medical Device Import No. 033568
DHA05603356801
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular devices
E4210 Vascular catheters, cannula and tubes for cardiopulmonary vascular bypass
Imported from abroad
Dates and Status
Apr 20, 2020
Apr 20, 2025

