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ResMed AirStart Positive Airway Pressure Device - Taiwan Registration 22f22dfaa906c75ae922c54b01802b8a

Access comprehensive regulatory information for ResMed AirStart Positive Airway Pressure Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22f22dfaa906c75ae922c54b01802b8a 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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22f22dfaa906c75ae922c54b01802b8a
Registration Details
Taiwan FDA Registration: 22f22dfaa906c75ae922c54b01802b8a
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Device Details

ResMed AirStart Positive Airway Pressure Device
TW: ็‘žๆ€้‚ไบžๆฒป้”ๆฐฃ้“ๆญฃๅฃ“ๅ‘ผๅธๅ™จ
Risk Class 2
MD

Registration Details

22f22dfaa906c75ae922c54b01802b8a

Ministry of Health Medical Device Import No. 029135

DHA05602913507

Company Information

Australia

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

Dec 08, 2016

Dec 08, 2026