Pure Global

"Medtronic" femoral arterial/venous cannula - Taiwan Registration bf591e1b4b45c365317b1ab51fa7e50a

Access comprehensive regulatory information for "Medtronic" femoral arterial/venous cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf591e1b4b45c365317b1ab51fa7e50a and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (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 Database
Powered by Pure Global AI
89,000+ Devices
bf591e1b4b45c365317b1ab51fa7e50a
Registration Details
Taiwan FDA Registration: bf591e1b4b45c365317b1ab51fa7e50a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medtronic" femoral arterial/venous cannula
TW: โ€œ็พŽๆ•ฆๅŠ›โ€่‚กๅ‹•/้œ่„ˆๅฅ—็ฎก
Risk Class 2
Cancelled

Registration Details

bf591e1b4b45c365317b1ab51fa7e50a

DHA00602205902

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing

import

Dates and Status

Feb 16, 2011

Feb 16, 2021

Oct 12, 2023

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€