"Leishi" sputum coughing auxiliary equipment - Taiwan Registration 4ad698bdc52c74bde9fb31c563484996
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 4ad698bdc52c74bde9fb31c563484996 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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
D Anesthesiology
D.5905 Non-continuous respirators
import
Dates and Status
Oct 17, 2011
Oct 17, 2016
Apr 25, 2018
Cancellation Information
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