PARAINFLUENZA VIRUS - ANVISA Registration 80254180239
Access comprehensive regulatory information for PARAINFLUENZA VIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80254180239 and manufactured by REMEL INC.. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including R-BIOPHARMA AG, OXOID (ELY) LIMITED, 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.
Device Details
Registration Details
80254180239
25351151355201701
04930429000139
Company Information
Dates and Status
Apr 24, 2017
VIGENTE
09/18/2025 19:00:01
VÍRUS PARAINFLUENZA
VIASURE Parainfluenza Real Time PCR Detection Kit
CERTEST BIOTEC, S.L.
10355870436
Aug 11, 2022
VÍRUS PARAINFLUENZA
IMAGEN PARAINFLUENZA VIRUS TYPES 1,2,3
OXOID (ELY) LIMITED
80254180267
Apr 24, 2017
VÍRUS PARAINFLUENZA
IMAGEN PARAINFLUENZA VIRUS GROUP (TYPES 1,2,3)
OXOID (ELY) LIMITED.
80254180282
Apr 24, 2017
VÍRUS PARAINFLUENZA
Ridascreen Parainfluenza 1, 2, 3 IgG
R-BIOPHARMA AG
80213250552
Mar 31, 2014
VÍRUS PARAINFLUENZA
Ridascreen Parainfluenza 1, 2, 3 IgA
R-BIOPHARMA AG
80213250545
Mar 31, 2014