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“Airon” pNeuton Ventilator System - Taiwan Registration 9460a968a4783fdadc0aa75313ce9204

Access comprehensive regulatory information for “Airon” pNeuton 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 9460a968a4783fdadc0aa75313ce9204 and manufactured by Airon Corporation. The authorized representative in Taiwan is TRANSCORE TAIWAN 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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9460a968a4783fdadc0aa75313ce9204
Registration Details
Taiwan FDA Registration: 9460a968a4783fdadc0aa75313ce9204
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Device Details

“Airon” pNeuton Ventilator System
TW: “愛龍”悠騰呼吸器系統
Risk Class 2
MD

Registration Details

9460a968a4783fdadc0aa75313ce9204

Ministry of Health Medical Device Import No. 028504

DHA05602850407

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

Apr 08, 2016

Apr 08, 2026