“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.
Device Details
Registration Details
ccb59a24175576c7ede3d9e8bff70ff3
Ministry of Health Medical Device Import No. 027593
DHA05602759301
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

