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“ResMed” AirCurve 10 VAuto Positive Airway Pressure Device - Taiwan Registration f5117fcbd98dcbe79b97fdf19ccc8d57

Access comprehensive regulatory information for “ResMed” AirCurve 10 VAuto 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 f5117fcbd98dcbe79b97fdf19ccc8d57 and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..

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f5117fcbd98dcbe79b97fdf19ccc8d57
Registration Details
Taiwan FDA Registration: f5117fcbd98dcbe79b97fdf19ccc8d57
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Device Details

“ResMed” AirCurve 10 VAuto Positive Airway Pressure Device
TW: “瑞思邁”艾克舒氣道正壓呼吸器
Risk Class 2
MD

Registration Details

f5117fcbd98dcbe79b97fdf19ccc8d57

Ministry of Health Medical Device Import No. 032558

DHA05603255806

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

Apr 09, 2019

Apr 09, 2024