"Leishi" Dream Nose Mask - Taiwan Registration 37aa58ed38c7b6ee53b6d8eff133fa01
Access comprehensive regulatory information for "Leishi" Dream Nose Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37aa58ed38c7b6ee53b6d8eff133fa01 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
37aa58ed38c7b6ee53b6d8eff133fa01
DHA05603658901
Product Details
Details are as detailed as approved Chinese instructions
D Anesthesiology
D.5905 Non-continuous respirators
Input;; Contract manufacturing
Dates and Status
Aug 30, 2023
Aug 30, 2028

