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“ResMed” Positive Airway Pressure Device, bi-level - Taiwan Registration 6b97a6e5c59053f77b79d4b02f1e372b

Access comprehensive regulatory information for “ResMed” Positive Airway Pressure Device, bi-level in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b97a6e5c59053f77b79d4b02f1e372b 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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6b97a6e5c59053f77b79d4b02f1e372b
Registration Details
Taiwan FDA Registration: 6b97a6e5c59053f77b79d4b02f1e372b
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Device Details

“ResMed” Positive Airway Pressure Device, bi-level
TW: “瑞思邁”氣道正壓呼吸輔助器
Risk Class 2
MD

Registration Details

6b97a6e5c59053f77b79d4b02f1e372b

Ministry of Health Medical Device Import No. 027285

DHA05602728503

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

May 06, 2015

May 06, 2025