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“ResMed” Bilevel Positive Airway Pressure Device - Taiwan Registration e2deaae74b746a8e543a31db24820728

Access comprehensive regulatory information for “ResMed” Bilevel 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 e2deaae74b746a8e543a31db24820728 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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e2deaae74b746a8e543a31db24820728
Registration Details
Taiwan FDA Registration: e2deaae74b746a8e543a31db24820728
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Device Details

“ResMed” Bilevel Positive Airway Pressure Device
TW: “瑞思邁”雙氣道正壓呼吸輔助器
Risk Class 2
MD

Registration Details

e2deaae74b746a8e543a31db24820728

Ministry of Health Medical Device Import No. 029265

DHA05602926507

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

Jan 05, 2017

Jan 05, 2027

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