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“Fukuda” Patient Monitor - Taiwan Registration 27532f5f9ce038d2abcf4089e35e8e04

Access comprehensive regulatory information for “Fukuda” Patient Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27532f5f9ce038d2abcf4089e35e8e04 and manufactured by BRITEMED TECHNOLOGY INC.. The authorized representative in Taiwan is BRITEMED TECHNOLOGY 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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27532f5f9ce038d2abcf4089e35e8e04
Registration Details
Taiwan FDA Registration: 27532f5f9ce038d2abcf4089e35e8e04
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Device Details

“Fukuda” Patient Monitor
TW: “福田”生理監護儀
Risk Class 2
MD

Registration Details

27532f5f9ce038d2abcf4089e35e8e04

Ministry of Health Medical Device Manufacturing No. 006413

Company Information

Taiwan, Province of China

Product Details

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

E Cardiovascular devices

E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)

Produced in Taiwan, China

Dates and Status

May 01, 2019

May 01, 2024