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“BALTON”River CTO Coronary Angioplasty Cathether - Taiwan Registration 511bc36cda448796950f07f9d0785daf

Access comprehensive regulatory information for “BALTON”River CTO Coronary Angioplasty Cathether in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 511bc36cda448796950f07f9d0785daf 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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511bc36cda448796950f07f9d0785daf
Registration Details
Taiwan FDA Registration: 511bc36cda448796950f07f9d0785daf
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Device Details

“BALTON”River CTO Coronary Angioplasty Cathether
TW: “拜登”羅凡賽冠狀動脈慢性阻塞擴張導管
Risk Class 2
MD

Registration Details

511bc36cda448796950f07f9d0785daf

Ministry of Health Medical Device Import No. 034624

DHA05603462403

Company Information

Poland

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E0005 Percutaneous puncture of the coronary ductus

Imported from abroad

Dates and Status

Oct 03, 2022

Oct 03, 2027