Pure Global

"Bud" Congust 40 percutaneous puncture angioplasty catheter - Taiwan Registration 43de174377002c82f734e6094c8013ab

Access comprehensive regulatory information for "Bud" Congust 40 percutaneous puncture angioplasty catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43de174377002c82f734e6094c8013ab and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., 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
43de174377002c82f734e6094c8013ab
Registration Details
Taiwan FDA Registration: 43de174377002c82f734e6094c8013ab
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Bud" Congust 40 percutaneous puncture angioplasty catheter
TW: โ€œๅทดๅพทโ€ๅบทๆ ผๆ–ฏ็‰น40็ถ“็šฎ็ฉฟๅˆบ่ก€็ฎกๆˆๅฝข่ก“ๅฐŽ็ฎก
Risk Class 2

Registration Details

43de174377002c82f734e6094c8013ab

DHA05602704509

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Mar 11, 2015

Mar 11, 2030