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“Fisher & Paykel” High Flow Heated Respiratory Humidifier - Taiwan Registration 03dcacb0b155781e98c4f943f150b3a5

Access comprehensive regulatory information for “Fisher & Paykel” High Flow Heated Respiratory Humidifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03dcacb0b155781e98c4f943f150b3a5 and manufactured by FISHER & PAYKEL HEALTHCARE LIMITED. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).

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03dcacb0b155781e98c4f943f150b3a5
Registration Details
Taiwan FDA Registration: 03dcacb0b155781e98c4f943f150b3a5
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Device Details

“Fisher & Paykel” High Flow Heated Respiratory Humidifier
TW: “費雪派克”高流量加熱式呼吸加濕器
Risk Class 2
MD

Registration Details

03dcacb0b155781e98c4f943f150b3a5

Ministry of Health Medical Device Import No. 029121

DHA05602912109

Product Details

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

D Devices for anesthesiology

D5450 Gas humidifier for respirators

Imported from abroad

Dates and Status

Nov 24, 2016

Nov 24, 2026