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“OMNIMATE” MANUAL RESUSCITATOR AND ACCESSORIES - Taiwan Registration c9fa24941bf57c5f1851fc342df2156f

Access comprehensive regulatory information for “OMNIMATE” MANUAL RESUSCITATOR AND ACCESSORIES in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c9fa24941bf57c5f1851fc342df2156f and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE 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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c9fa24941bf57c5f1851fc342df2156f
Registration Details
Taiwan FDA Registration: c9fa24941bf57c5f1851fc342df2156f
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Device Details

“OMNIMATE” MANUAL RESUSCITATOR AND ACCESSORIES
TW: “廣鎬”人工呼吸器及其配件
Risk Class 2
MD

Registration Details

c9fa24941bf57c5f1851fc342df2156f

Ministry of Health Medical Device Manufacturing No. 006238

Company Information

Taiwan, Province of China

Product Details

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

D Devices for anesthesiology

D5915 Manual Emergency Respirator

Produced in Taiwan, China

Dates and Status

Nov 27, 2018

Nov 27, 2028