Pure Global

"Serucon" coronary angioplasty balloon catheter - Taiwan Registration b0e520aafbdad80369953bd730bb35bd

Access comprehensive regulatory information for "Serucon" coronary angioplasty balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0e520aafbdad80369953bd730bb35bd and manufactured by MedAlliance LLC;; MedAlliance CardioVascular SA. The authorized representative in Taiwan is REGISTAR 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
b0e520aafbdad80369953bd730bb35bd
Registration Details
Taiwan FDA Registration: b0e520aafbdad80369953bd730bb35bd
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Serucon" coronary angioplasty balloon catheter
TW: โ€œ็‘Ÿ็’ๆฝฏโ€ๅ† ็‹€ๅ‹•่„ˆๆˆๅฝข่ก“็ƒๅ›ŠๅฐŽ็ฎก
Risk Class 2

Registration Details

b0e520aafbdad80369953bd730bb35bd

DHA05603579407

Company Information

United States;;Switzerland

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.0005.

import

Dates and Status

Sep 17, 2022

Sep 17, 2027