“ResMed” Bilevel Positive Airway Pressure Device - Taiwan Registration ced423de7f946994ba81732a494fb5c5
Access comprehensive regulatory information for “ResMed” Bilevel Positive Airway Pressure Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ced423de7f946994ba81732a494fb5c5 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
ced423de7f946994ba81732a494fb5c5
Ministry of Health Medical Device Import No. 029421
DHA05602942108
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
Mar 23, 2017
Mar 23, 2027

