HEMOGLOBIN SUBTYPE - NEONATAL SCREENING - ANVISA Registration 80416660140
Access comprehensive regulatory information for HEMOGLOBIN SUBTYPE - NEONATAL SCREENING in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80416660140 and manufactured by manufacturer not specified. The registration is held by SEBIA IMPORTAÇÕES COMERCIALIZAÇÃO E DISTRIBUIÇÃO DE APARELHOS E REATIVOS PARA DIAGNÓSTICO IN VITRO LTDA. with validity until Mar 06, 2033.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA, WALLAC OY, 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
80416660140
25351482972202275
08576331000186
Company Information
Dates and Status
Mar 06, 2023
06/03/2033
09/18/2025 19:00:01
HEMOGLOBINA SUBTIPO - TRIAGEM NEONATAL
RESOLVE™ Hemoglobin Kit
Not specified
10298910184
Oct 21, 2024
HEMOGLOBINA SUBTIPO - TRIAGEM NEONATAL
RESOLVE™ Hemoglobin Kit
WALLAC OY
10298910184
Oct 21, 2024
HEMOGLOBINA SUBTIPO - TRIAGEM NEONATAL
KIT ULTRA SCREENING GENESYS
TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA
81733730001
May 20, 2019
HEMOGLOBINA SUBTIPO - TRIAGEM NEONATAL
VARIANT nbs Sickle Cell Program
BIO-RAD LABORATORIES, INC
80020690277
Jan 30, 2012
HEMOGLOBINA SUBTIPO - TRIAGEM NEONATAL
VARIANT nbs Sickle Cell Program
Not specified
80020690277
Jan 30, 2012

