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“MEDIANA” Automated External Defibrillator - Taiwan Registration a2feedb4eecc77cbdae2182de93c7f21

Access comprehensive regulatory information for “MEDIANA” Automated External Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a2feedb4eecc77cbdae2182de93c7f21 and manufactured by MEDIANA CO., LTD.. The authorized representative in Taiwan is DERLIN BIOMEDICAL 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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a2feedb4eecc77cbdae2182de93c7f21
Registration Details
Taiwan FDA Registration: a2feedb4eecc77cbdae2182de93c7f21
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Device Details

“MEDIANA” Automated External Defibrillator
TW: “玫迪納”自動體外心臟除顫器
Risk Class 3
MD

Registration Details

a2feedb4eecc77cbdae2182de93c7f21

Ministry of Health Medical Device Import No. 035013

DHA05603501305

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E5310 Automated External Defibrillator System

Imported from abroad

Dates and Status

Oct 28, 2021

Oct 28, 2026