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“Japan Lifeline” BeeAT Atrial Cardioversion Catheter - Taiwan Registration 5aba8298360c8cef8c7eaf7fb49891d1

Access comprehensive regulatory information for “Japan Lifeline” BeeAT Atrial Cardioversion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5aba8298360c8cef8c7eaf7fb49891d1 and manufactured by Japan Lifeline Co., Ltd. Toda Factory. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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5aba8298360c8cef8c7eaf7fb49891d1
Registration Details
Taiwan FDA Registration: 5aba8298360c8cef8c7eaf7fb49891d1
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Device Details

“Japan Lifeline” BeeAT Atrial Cardioversion Catheter
TW: “日本來富恩” 心腔內除顫導管
Risk Class 3
MD

Registration Details

5aba8298360c8cef8c7eaf7fb49891d1

Ministry of Health Medical Device Import No. 025948

DHA05602594802

Company Information

Product Details

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

E Cardiovascular devices

Imported from abroad

Dates and Status

May 28, 2014

May 28, 2024