“ResMed” AirFit Mask - Taiwan Registration 51996567455e2388ba5ff0ee9e741ddc
Access comprehensive regulatory information for “ResMed” AirFit Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51996567455e2388ba5ff0ee9e741ddc and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ResMed Pty 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.
Device Details
Registration Details
51996567455e2388ba5ff0ee9e741ddc
Ministry of Health Medical Device Import No. 034746
DHA05603474604
Product Details
Details are as detailed as approved Chinese instructions
D Devices for anesthesiology
D5895 Continuous breathing apparatus
Imported from abroad
Dates and Status
Jun 30, 2021
Jun 30, 2026

