STREPTOCOCCUS - ANVISA Registration 10339840518
Access comprehensive regulatory information for STREPTOCOCCUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10339840518 and manufactured by manufacturer not specified. The registration is held by DIASORIN LTDA with validity until Oct 14, 2029.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including VEDALAB, Eco Diagnostica 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
10339840518
25351567889201970
01896764000170
Company Information
Dates and Status
Oct 14, 2019
14/10/2029
09/18/2025 19:00:01
STREPTOCOCCUS
Teste Rápido de Antígeno Strep A
HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.
81472060046
Jul 28, 2025
STREPTOCOCCUS
Teste Rápido de Antígeno Strep A
Not specified
81472060046
Jul 28, 2025
STREPTOCOCCUS
Kit Detecção qPCR para Streptococcus do Grupo B
SANSURE BIOTECH INC
80680250056
Apr 28, 2025
STREPTOCOCCUS
Kit Detecção qPCR para Streptococcus do Grupo B
Not specified
80680250056
Apr 28, 2025
STREPTOCOCCUS
LIAISON® S. pneumoniae Ag
DIASORIN ITALIA S.P.A.
10339840562
Mar 31, 2025

