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“CU Medical” Semi-automated External Defibrillator - Taiwan Registration 40e211e7ba94a243b7939b158b08a754

Access comprehensive regulatory information for “CU Medical” Semi-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 40e211e7ba94a243b7939b158b08a754 and manufactured by CU Medical System, Inc.. The authorized representative in Taiwan is ACARE TECHNOLOGY 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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40e211e7ba94a243b7939b158b08a754
Registration Details
Taiwan FDA Registration: 40e211e7ba94a243b7939b158b08a754
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Device Details

“CU Medical” Semi-automated External Defibrillator
TW: “希安”半自動體外心臟去顫器
Risk Class 3
MD

Registration Details

40e211e7ba94a243b7939b158b08a754

Ministry of Health Medical Device Import No. 029387

DHA05602938708

Company Information

Korea, Republic of

Product Details

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

E Cardiovascular devices

E5310 Automated External Defibrillator

Imported from abroad

Dates and Status

Feb 14, 2017

Feb 14, 2022