“RAYBOW” Fiberoptic Dental Light Source (Non-Sterile)　 - Taiwan Registration b49f480aa0d0521e4d04916cebc11a60

Access comprehensive regulatory information for “RAYBOW” Fiberoptic Dental Light Source (Non-Sterile)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b49f480aa0d0521e4d04916cebc11a60 and manufactured by RAYBOW GMBH. The authorized representative in Taiwan is PULLIER CO., LTD..

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.