“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.
Device Details
Registration Details
bab889cb8b0efe80646fac3380983b79
Ministry of Health Medical Device Import No. 032608
DHA05603260808
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

