“ResMed” POSITIVE AIRWAY PRESSURE THERAPY DEVICE - Taiwan Registration 36a3aeafe3dbf594c94a31a977b7958b
Access comprehensive regulatory information for “ResMed” POSITIVE AIRWAY PRESSURE THERAPY DEVICE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36a3aeafe3dbf594c94a31a977b7958b and manufactured by RESMED LIMITED. 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
36a3aeafe3dbf594c94a31a977b7958b
Ministry of Health Medical Device Import No. 029967
DHA05602996700
Product Details
For details, it is Chinese approved copy of the imitation order
D Devices for anesthesiology
D5895 Continuous breathing apparatus
Imported from abroad
Dates and Status
Jul 12, 2017
Jul 12, 2022

