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“RESMED”Therapeutic humidifier for home use (Non-Sterile) - Taiwan Registration 955396657e885c2b8c21d4bebe9f7d57

Access comprehensive regulatory information for “RESMED”Therapeutic humidifier for home use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 955396657e885c2b8c21d4bebe9f7d57 and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..

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955396657e885c2b8c21d4bebe9f7d57
Registration Details
Taiwan FDA Registration: 955396657e885c2b8c21d4bebe9f7d57
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Device Details

“RESMED”Therapeutic humidifier for home use (Non-Sterile)
TW: “瑞思邁”居家用治療潮濕器 (未滅菌)
Risk Class 1
MD

Registration Details

955396657e885c2b8c21d4bebe9f7d57

Ministry of Health Medical Device Import No. 013439

DHA09401343901

Company Information

Australia

Product Details

Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Household Treatment Moisturizer (D.5460)".

D Devices for anesthesiology

D5460 Household Therapeutic Moisturizer

Imported from abroad

Dates and Status

Sep 18, 2013

Sep 18, 2028