Patient lift/transfer device - ANVISA Registration 82255340007

Access comprehensive regulatory information for Patient lift/transfer device in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82255340007 and manufactured by FOSHAN DONGFANG MEDICAL EQUIPMENT MANUFACTORY (LTD.). The registration is held by LEMON BRASIL COMERCIO ATACADISTA DE ELETRONICOS E PRODUTOS EM GERAL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including ZHONGSHAN JIALE REHABILITATION MEDICAL EQUIPMENT CO., LTD, ARPE MEDICAL REPRESENTACAO, COMERCIO E ASSISTENCIA TECNICA LTDA, and 4 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.