Taiwan FDA registration bab889cb8b0efe80646fac3380983b79

“Fisher & Paykel” Respiratory Humidifier

TW: “費雪派克”呼吸器用加熱加溼系統
Taiwan flagTaiwan·Risk Class 2·MD·FISHER & PAYKEL HEALTHCARE LTD.·Registered May 20, 2019 – May 20, 2024Expired
Registration details
Analysis ID
bab889cb8b0efe80646fac3380983b79
License Form
Ministry of Health Medical Device Import No. 032608
Customs Code
DHA05603260808
Company information
Manufacturer Country
New Zealand
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5450 Gas humidifier for respirators
Import Information
Imported from abroad
Dates and status
Registration Date
May 20, 2019
Expiry Date
May 20, 2024
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About this record

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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