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“ResMed” AirFit N30 for AirMini Mask - Taiwan Registration 9bcdd96126aa494d296dd333f5839e73

Access comprehensive regulatory information for “ResMed” AirFit N30 for AirMini Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9bcdd96126aa494d296dd333f5839e73 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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9bcdd96126aa494d296dd333f5839e73
Registration Details
Taiwan FDA Registration: 9bcdd96126aa494d296dd333f5839e73
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Device Details

“ResMed” AirFit N30 for AirMini Mask
TW: “瑞思邁”易適亞米面罩
Risk Class 2
MD

Registration Details

9bcdd96126aa494d296dd333f5839e73

Ministry of Health Medical Device Import No. 034731

DHA05603473104

Company Information

Australia

Product Details

Details are as detailed as approved Chinese instructions

D Devices for anesthesiology

D5895 Continuous breathing apparatus

Imported from abroad

Dates and Status

Jun 15, 2021

Jun 15, 2026