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“Fisher & Paykel” Respiratory Humidifier - Taiwan Registration 1844655ff8c0272e619f6dcd01dc38f2

Access comprehensive regulatory information for “Fisher & Paykel” 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 1844655ff8c0272e619f6dcd01dc38f2 and manufactured by FISHER & PAYKEL HEALTHCARE LIMITED. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FISHER & PAYKEL HEALTHCARE 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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1844655ff8c0272e619f6dcd01dc38f2
Registration Details
Taiwan FDA Registration: 1844655ff8c0272e619f6dcd01dc38f2
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Device Details

“Fisher & Paykel” Respiratory Humidifier
TW: “費雪派克”呼吸潮濕加熱器系統
Risk Class 2
MD

Registration Details

1844655ff8c0272e619f6dcd01dc38f2

Ministry of Health Medical Device Import No. 032780

DHA05603278007

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

Aug 01, 2019

Aug 01, 2024

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