“ResMed” Bilevel Positive Airway Pressure Device - Taiwan Registration e2deaae74b746a8e543a31db24820728
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 e2deaae74b746a8e543a31db24820728 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
e2deaae74b746a8e543a31db24820728
Ministry of Health Medical Device Import No. 029265
DHA05602926507
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
Jan 05, 2017
Jan 05, 2027

