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“ResMed” Continuous Positive Airway Pressure device - Taiwan Registration 8b7607acb7bceff01da4a7d95b79a836

Access comprehensive regulatory information for “ResMed” Continuous 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 8b7607acb7bceff01da4a7d95b79a836 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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8b7607acb7bceff01da4a7d95b79a836
Registration Details
Taiwan FDA Registration: 8b7607acb7bceff01da4a7d95b79a836
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Device Details

“ResMed” Continuous Positive Airway Pressure device
TW: “瑞思邁”連續性氣道正壓呼吸器
Risk Class 2
MD

Registration Details

8b7607acb7bceff01da4a7d95b79a836

Ministry of Health Medical Device Import No. 027422

DHA05602742200

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

Jun 11, 2015

Jun 11, 2025