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Klux Automated External Defibrillator - Taiwan Registration 72807359b52d5ca7bdf21ba86a7bce4a

Access comprehensive regulatory information for Klux 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 72807359b52d5ca7bdf21ba86a7bce4a and manufactured by KLUX CO., LTD.. The authorized representative in Taiwan is KLUX 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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72807359b52d5ca7bdf21ba86a7bce4a
Registration Details
Taiwan FDA Registration: 72807359b52d5ca7bdf21ba86a7bce4a
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Device Details

Klux Automated External Defibrillator
TW: ๅ‡ฑๆจ‚ๆ–ฏ่‡ชๅ‹•้ซ”ๅค–ๅฟƒ่‡ŸๅŽป้กซ้›ปๆ“Šๅ™จ
Risk Class 3
MD

Registration Details

72807359b52d5ca7bdf21ba86a7bce4a

Ministry of Health Medical Device Manufacturing No. 005119

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 15, 2015

Sep 15, 2025