LEISHMANIA SP - ANVISA Registration 80524900058
Access comprehensive regulatory information for LEISHMANIA 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 80524900058 and manufactured by manufacturer not specified. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Jun 12, 2027.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including VIRCELL S.L., ADVAGEN BIOTECH LTDA, 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.
Related Devices (2)
Registration Details
80524900058
25351098537201706
09593438000103
Company Information
Dates and Status
Jun 12, 2017
12/06/2027
09/18/2025 19:00:01
LEISHMANIA SP
Kit IBMP Biomol Leishmaniose
INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ
80780040026
May 19, 2025
LEISHMANIA SP
VIASURE Leishmania Real Time PCR Detection Kit
CERTEST BIOTEC, S.L.
82149920105
Feb 17, 2025
LEISHMANIA SP
VIASURE Leishmania Real Time PCR Detection Kit
Not specified
82149920105
Feb 17, 2025
LEISHMANIA SP
TR LVH - Bio-Manguinhos
Fundação Oswaldo Cruz - Instituto de Tecnologia em Imunobiológicos -
80142170070
Nov 11, 2024
LEISHMANIA SP
FASTLINE LEISHMANIA IgG/IgM
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA
80105220183
Apr 08, 2024

