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“ResMed” AirMini system - Taiwan Registration 4fb47e24a85a0aea2bcd83553d572772

Access comprehensive regulatory information for “ResMed” AirMini system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4fb47e24a85a0aea2bcd83553d572772 and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED 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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4fb47e24a85a0aea2bcd83553d572772
Registration Details
Taiwan FDA Registration: 4fb47e24a85a0aea2bcd83553d572772
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Device Details

“ResMed” AirMini system
TW: “瑞思邁”亞米正壓呼吸器
Risk Class 2
MD

Registration Details

4fb47e24a85a0aea2bcd83553d572772

Ministry of Health Medical Device Import No. 030639

DHA05603063909

Company Information

Australia

Product Details

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

D Devices for anesthesiology

D5895 Continuous breathing apparatus and accessories

Imported from abroad

Dates and Status

Jan 02, 2018

Jan 02, 2028