"Leishi" bronchial examination elbow - Taiwan Registration d09bcb19f8853baab9d96d3e752ccd46
Access comprehensive regulatory information for "Leishi" bronchial examination elbow in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d09bcb19f8853baab9d96d3e752ccd46 and manufactured by 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.
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d09bcb19f8853baab9d96d3e752ccd46
Registration Details
Taiwan FDA Registration: d09bcb19f8853baab9d96d3e752ccd46
Device Details
"Leishi" bronchial examination elbow
TW: โ็ฃไปโๆฏๆฐฃ็ฎกๆชขๆฅๅฝ็ฎก
Risk Class 2

