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“ResMed” POSITIVE AIRWAY PRESSURE THERAPY DEVICE - Taiwan Registration 36a3aeafe3dbf594c94a31a977b7958b

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 36a3aeafe3dbf594c94a31a977b7958b and manufactured by RESMED LIMITED. 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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36a3aeafe3dbf594c94a31a977b7958b
Registration Details
Taiwan FDA Registration: 36a3aeafe3dbf594c94a31a977b7958b
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Device Details

“ResMed” POSITIVE AIRWAY PRESSURE THERAPY DEVICE
TW: “瑞思邁”雙氣道正壓呼吸治療器
Risk Class 2
MD

Registration Details

36a3aeafe3dbf594c94a31a977b7958b

Ministry of Health Medical Device Import No. 029967

DHA05602996700

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

Jul 12, 2017

Jul 12, 2022

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