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“GE” Ventilator System - Taiwan Registration ccb59a24175576c7ede3d9e8bff70ff3

Access comprehensive regulatory information for “GE” Ventilator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ccb59a24175576c7ede3d9e8bff70ff3 and manufactured by DATEX-OHMEDA INC.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, 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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ccb59a24175576c7ede3d9e8bff70ff3
Registration Details
Taiwan FDA Registration: ccb59a24175576c7ede3d9e8bff70ff3
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Device Details

“GE” Ventilator System
TW: “奇異”呼吸系統
Risk Class 2
MD

Registration Details

ccb59a24175576c7ede3d9e8bff70ff3

Ministry of Health Medical Device Import No. 027593

DHA05602759301

Company Information

United States

Product Details

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

D Devices for anesthesiology

D5895 Continuous breathing apparatus

Imported from abroad

Dates and Status

Aug 14, 2015

Aug 14, 2025