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“Fisher & Paykel” Respiratory Humidifier - Taiwan Registration bab889cb8b0efe80646fac3380983b79

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 bab889cb8b0efe80646fac3380983b79 and manufactured by FISHER & PAYKEL HEALTHCARE LTD.. 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 LIMITED, 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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bab889cb8b0efe80646fac3380983b79
Registration Details
Taiwan FDA Registration: bab889cb8b0efe80646fac3380983b79
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Device Details

“Fisher & Paykel” Respiratory Humidifier
TW: “費雪派克”呼吸器用加熱加溼系統
Risk Class 2
MD

Registration Details

bab889cb8b0efe80646fac3380983b79

Ministry of Health Medical Device Import No. 032608

DHA05603260808

Company Information

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

May 20, 2019

May 20, 2024

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