Руководство по сертификации устройств для светодиодной терапии: Как проверить FDA, CE/МЛУ, Мдл, TGA, Iso, MDSAP, UL, и протоколы испытаний
TL;DR (for B2B buyers) First classify the product: a medical / therapeutic LED device and a general beauty electrical appliance do not need the same evidence package. Do not stop at “FDA registered.” Ask for the FDA 510(k) number, covered models, предполагаемое использование, product codes, and clearance documentation. For regulated-market products, verify market records and […]