MYOGLOBIN - ANVISA Registration 80474870167
Access comprehensive regulatory information for MYOGLOBIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80474870167 and manufactured by manufacturer not specified. The registration is held by BIOSUL PRODUTOS DIAGNOSTICOS LTDA - ME with validity until Sep 08, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including HANGZHOU ALLTEST BIOTECH CO. LTD, KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS 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
80474870167
25351098582202563
05905525000190
Company Information
Dates and Status
Sep 08, 2025
08/09/2035
09/18/2025 19:00:01
HANGZHOU ALLTEST BIOTECH CO. LTDโข China
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDAโข Brazil
ROCHE DIAGNOSTICS GMBHโข Germany
RADIOMETER MEDICAL APSโข Denmark
BODITECH MED INC.โข South Korea
MIOGLOBINA
Famรญlia AFIAS Myoglobin Neo
BODITECH MED INC.
10350840479
Jun 23, 2025
MIOGLOBINA
Famรญlia AFIAS Myoglobin Neo
Not specified
10350840479
Jun 23, 2025
MIOGLOBINA
Famรญlia AQT90 FLEX Myo
RADIOMETER MEDICAL APS
10033121079
Jun 02, 2025
MIOGLOBINA
Famรญlia AQT90 FLEX Myo
Not specified
10033121079
Jun 02, 2025
MIOGLOBINA
Teste Rรกpido Mioglobina
HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.
81472060042
May 26, 2025

