"SKED" Manual patient transfer device (Non-Sterile) - Taiwan Registration 89d6325a5218e2234fe2968bf75d5307

Access comprehensive regulatory information for "SKED" Manual patient transfer device (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 89d6325a5218e2234fe2968bf75d5307 and manufactured by SKEDCO, INC.. The authorized representative in Taiwan is RAY LONG OUTDOORS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SKEDCO,INC, SKEDCO, INC., and 3 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.