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“Resmed” AirView Software - Taiwan Registration 62b0502780cdc67c97f9e49ff9f93883

Access comprehensive regulatory information for “Resmed” AirView Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 62b0502780cdc67c97f9e49ff9f93883 and manufactured by ResMed Corp. 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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62b0502780cdc67c97f9e49ff9f93883
Registration Details
Taiwan FDA Registration: 62b0502780cdc67c97f9e49ff9f93883
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Device Details

“Resmed” AirView Software
TW: “瑞思邁”睡眠呼吸記錄軟體
Risk Class 2
MD

Registration Details

62b0502780cdc67c97f9e49ff9f93883

Ministry of Health Medical Device Import No. 032304

DHA05603230401

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

Imported from abroad

Dates and Status

Mar 19, 2019

Mar 19, 2029