"Leishi" sputum coughing auxiliary equipment - Taiwan Registration a626ef09c62161ff8e0ab026ef625190

Access comprehensive regulatory information for "Leishi" sputum coughing auxiliary equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a626ef09c62161ff8e0ab026ef625190 and manufactured by Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESPIRONICS INC., 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.