"Leishi" oxygen concentrator - Taiwan Registration d3817474282e20e68456e9cfc61e4e70
Access comprehensive regulatory information for "Leishi" oxygen concentrator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3817474282e20e68456e9cfc61e4e70 and manufactured by Flextronics Manufacturing Juarez S. de R.L. de C.V.;; RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including RESPIRONICS INC.;; Respironics, Inc., Respironics, Inc., and 2 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
d3817474282e20e68456e9cfc61e4e70
DHA05602641205
Product Details
For details, it is Chinese approved copy of the imitation order
D Anesthesiology
D.5440 Portable Oxygen Generator
Contract manufacturing;; input
Dates and Status
Jul 28, 2014
Jul 28, 2029

