F&P 950 breathing humidity heater system - Taiwan Registration 0bd78afa4ae1d5b80cddefb576ae15de

Access comprehensive regulatory information for F&P 950 breathing humidity heater system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0bd78afa4ae1d5b80cddefb576ae15de 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. 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.