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“Biosense Webster” nMARQ Multi-Channel RF Generator - Taiwan Registration 9dad7430347f3bb995cba3b9b87286c7

Access comprehensive regulatory information for “Biosense Webster” nMARQ Multi-Channel RF Generator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9dad7430347f3bb995cba3b9b87286c7 and manufactured by BIOSENSE WEBSTER, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL 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.

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9dad7430347f3bb995cba3b9b87286c7
Registration Details
Taiwan FDA Registration: 9dad7430347f3bb995cba3b9b87286c7
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Device Details

“Biosense Webster” nMARQ Multi-Channel RF Generator
TW: “百歐森偉伯斯特”安瑪可多通道心臟射頻電燒儀
Risk Class 3
MD
Cancelled

Registration Details

9dad7430347f3bb995cba3b9b87286c7

Ministry of Health Medical Device Import No. 027847

DHA05602784706

Company Information

United States

Product Details

E Cardiovascular devices

Imported from abroad

Dates and Status

Nov 11, 2015

Nov 11, 2020

Nov 22, 2018

Cancellation Information

Logged out

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