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“ResMed” Bilevel Positive Airway Pressure Device - Taiwan Registration ced423de7f946994ba81732a494fb5c5

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 ced423de7f946994ba81732a494fb5c5 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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ced423de7f946994ba81732a494fb5c5
Registration Details
Taiwan FDA Registration: ced423de7f946994ba81732a494fb5c5
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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

ced423de7f946994ba81732a494fb5c5

Ministry of Health Medical Device Import No. 029421

DHA05602942108

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

Mar 23, 2017

Mar 23, 2027

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