LEPTOSPIRA SP - ANVISA Registration 10259610257

Access comprehensive regulatory information for LEPTOSPIRA SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10259610257 and manufactured by VIRCELL S.L.. The registration is held by MEDIVAX INDÚSTRIA E COMÉRCIO LTDA with validity until Jun 09, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including INSTITUT VIRION\SERION GMBH, HANGZHOU ALLTEST BIOTECH CO. LTD, 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.