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“ResMed” Positive Airway Pressure Therapy Device - Taiwan Registration 4b2daa77fd6ca02c8a3fd3ab51d7a860

Access comprehensive regulatory information for “ResMed” Positive Airway Pressure Therapy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b2daa77fd6ca02c8a3fd3ab51d7a860 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 LIMITED, 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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4b2daa77fd6ca02c8a3fd3ab51d7a860
Registration Details
Taiwan FDA Registration: 4b2daa77fd6ca02c8a3fd3ab51d7a860
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Device Details

“ResMed” Positive Airway Pressure Therapy Device
TW: “瑞思邁”氣道正壓呼吸治療系統
Risk Class 2
MD

Registration Details

4b2daa77fd6ca02c8a3fd3ab51d7a860

Ministry of Health Medical Device Import No. 028649

DHA05602864907

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

Aug 01, 2016

Aug 01, 2026

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