Pure Global

“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.

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 Database
Powered by Pure Global AI
89,000+ Devices
012bc31932153d59e7edbe307004d8a4
Registration Details
Taiwan FDA Registration: 012bc31932153d59e7edbe307004d8a4
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Fuji” AP-GRIPFLOW Circulation Perfusion Catheter
TW: “富士”主動脈循環灌注導管
Risk Class 2
MD

Registration Details

012bc31932153d59e7edbe307004d8a4

Ministry of Health Medical Device Import No. 033568

DHA05603356801

Company Information

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