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“RESMED” POSITIVE AIRWAY PRESSURE DEVICE - Taiwan Registration a757adf59b42e27e12e3f8d726d883ce

Access comprehensive regulatory information for “RESMED” 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 a757adf59b42e27e12e3f8d726d883ce and manufactured by RESMED LTD. The authorized representative in Taiwan is BROJAW INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ResMed Pty Ltd., and 2 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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a757adf59b42e27e12e3f8d726d883ce
Registration Details
Taiwan FDA Registration: a757adf59b42e27e12e3f8d726d883ce
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Device Details

“RESMED” POSITIVE AIRWAY PRESSURE DEVICE
TW: “瑞思邁”陽壓呼吸輔助器
Risk Class 2
MD
Cancelled

Registration Details

a757adf59b42e27e12e3f8d726d883ce

Ministry of Health Medical Device Import No. 027265

DHA05602726500

Company Information

Australia

Product Details

D Devices for anesthesiology

D5895 Continuous breathing apparatus

Imported from abroad

Dates and Status

Apr 21, 2015

Apr 21, 2020

Aug 05, 2022

Cancellation Information

Logged out

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