"KENDA" Abrasive device and accessories (Non-Sterile) - Taiwan Registration 4f778489a6e88106fd7c6379f9f73056

Access comprehensive regulatory information for "KENDA" Abrasive device and accessories (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 4f778489a6e88106fd7c6379f9f73056 and manufactured by KENDA AG. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including KENDA AG, KENDA AG. DENTAL MANUFACTURING, and 4 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.