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“ResMed” Quattro Air Non-Vented Full Face mask - Taiwan Registration 3ba796dcf74bd3e03a9b7bd2162121a4

Access comprehensive regulatory information for “ResMed” Quattro Air Non-Vented Full Face mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ba796dcf74bd3e03a9b7bd2162121a4 and manufactured by RESMED LIMITED. 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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Registration Details
Taiwan FDA Registration: 3ba796dcf74bd3e03a9b7bd2162121a4
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Device Details

“ResMed” Quattro Air Non-Vented Full Face mask
TW: “瑞思邁”卓越無通氣孔面罩
Risk Class 2
MD

Registration Details

3ba796dcf74bd3e03a9b7bd2162121a4

Ministry of Health Medical Device Import No. 032091

DHA05603209100

Company Information

Australia

Product Details

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

D Devices for anesthesiology

D5905 Discontinuous respirators

Imported from abroad

Dates and Status

Jan 28, 2019

Jan 28, 2024