Taiwan FDA registration 1844655ff8c0272e619f6dcd01dc38f2

“Fisher & Paykel” Respiratory Humidifier

TW: “費雪派克”呼吸潮濕加熱器系統
Taiwan flagTaiwan·Risk Class 2·MD·FISHER & PAYKEL HEALTHCARE LIMITED·Registered Aug 01, 2019 – Aug 01, 2024Expired
Registration details
Analysis ID
1844655ff8c0272e619f6dcd01dc38f2
License Form
Ministry of Health Medical Device Import No. 032780
Customs Code
DHA05603278007
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
Aug 01, 2019
Expiry Date
Aug 01, 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 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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