Devices - ANVISA Registration 80145110205

Access comprehensive regulatory information for Devices in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80145110205 and manufactured by FABRICADO POR: FRESENIUS KABI DEUTSCHLAND GMBH - ALEMANHA PARA FRESENIUS KABI AG. The registration is held by FRESENIUS KABI BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 4 related devices, regulatory compliance details, 5 companies making the same product including APPLIED MEDICAL TECHNOLOGY, INC, ATOS MEDICAL AB, and 5 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.