“LiteCure” LightForce Deep Tissue Laser Therapy System - Taiwan Registration 236acd5c7cfef70db8e8da87511bf92a

Access comprehensive regulatory information for “LiteCure” LightForce Deep Tissue Laser Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 236acd5c7cfef70db8e8da87511bf92a and manufactured by LITECURE, LLC. The authorized representative in Taiwan is CONTINUOUS INSTRUMENT 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.