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“ResMed” AirFit Mask - Taiwan Registration 51996567455e2388ba5ff0ee9e741ddc

Access comprehensive regulatory information for “ResMed” AirFit Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51996567455e2388ba5ff0ee9e741ddc 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, 1 companies making similar products including ResMed Pty Ltd, and 1 recent registrations in the same category. 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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51996567455e2388ba5ff0ee9e741ddc
Registration Details
Taiwan FDA Registration: 51996567455e2388ba5ff0ee9e741ddc
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Device Details

“ResMed” AirFit Mask
TW: “瑞思邁” 易適面罩
Risk Class 2
MD

Registration Details

51996567455e2388ba5ff0ee9e741ddc

Ministry of Health Medical Device Import No. 034746

DHA05603474604

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 30, 2021

Jun 30, 2026

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