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“LIFE ARK” AUTOMATED EXTERNAL DEFIBRILLATOR AND ACCESSORIES - Taiwan Registration 7232d15a10e6fcbda9c9b0e8ffe75191

Access comprehensive regulatory information for “LIFE ARK” AUTOMATED EXTERNAL DEFIBRILLATOR AND ACCESSORIES in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7232d15a10e6fcbda9c9b0e8ffe75191 and manufactured by DERMACARE BIOMED INC.. The authorized representative in Taiwan is DERMACARE BIOMED INC..

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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7232d15a10e6fcbda9c9b0e8ffe75191
Registration Details
Taiwan FDA Registration: 7232d15a10e6fcbda9c9b0e8ffe75191
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Device Details

“LIFE ARK” AUTOMATED EXTERNAL DEFIBRILLATOR AND ACCESSORIES
TW: “生命方舟”自動體外心臟電擊去顫器及附件
Risk Class 3
MD

Registration Details

7232d15a10e6fcbda9c9b0e8ffe75191

Ministry of Health Medical Device Manufacturing No. 005866

Company Information

Taiwan, Province of China

Product Details

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

E Cardiovascular devices

E5310 Automated External Defibrillator

Produced in Taiwan, China

Dates and Status

Sep 12, 2017

Sep 12, 2027