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“BALTON”Valvuloplasty catheter Valver - Taiwan Registration 7129d6ff4d05f97b70145008fba7f3cc

Access comprehensive regulatory information for “BALTON”Valvuloplasty catheter Valver in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7129d6ff4d05f97b70145008fba7f3cc and manufactured by Balton Sp.z o.o.. The authorized representative in Taiwan is CATHERINE CONSULTANTS 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.

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7129d6ff4d05f97b70145008fba7f3cc
Registration Details
Taiwan FDA Registration: 7129d6ff4d05f97b70145008fba7f3cc
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Device Details

“BALTON”Valvuloplasty catheter Valver
TW: “拜登”法菲心瓣膜成形導管
Risk Class 2
MD

Registration Details

7129d6ff4d05f97b70145008fba7f3cc

Ministry of Health Medical Device Import No. 034629

DHA05603462900

Company Information

Poland

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E1255 Aortic valvuloplasty balloon catheter

Imported from abroad

Dates and Status

Nov 30, 2022

Nov 30, 2027