"Leishi" Dream full mask - Taiwan Registration f26eb100d371c4ca66b739c823a66e3a
Access comprehensive regulatory information for "Leishi" Dream full mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f26eb100d371c4ca66b739c823a66e3a and manufactured by Philips de Costa Rica S.R.L.;; RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. 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
f26eb100d371c4ca66b739c823a66e3a
DHA05603658809
Product Details
Details are as detailed as approved Chinese instructions
D Anesthesiology
D.5905 Non-continuous respirators
Contract manufacturing;; input
Dates and Status
Aug 30, 2023
Aug 30, 2028

