CHIKUNGUNYA - ANVISA Registration 80345000254
Access comprehensive regulatory information for CHIKUNGUNYA in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80345000254 and manufactured by DIA PRO DIAGNOSTIC BIOPROBES S.R.L.. The registration is held by GOYAZES BIOTECNOLOGIA LTDA with validity until Jul 16, 2028.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including Eco Diagnostica Ltda, VIRCELL MICROBIOLOGISTS, 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.

Janaina dos Santos de Miranda
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Registration Details
80345000254
25351293676201815
05658906000111
Company Information
Dates and Status
Jul 16, 2018
16/07/2028
09/18/2025 19:00:01
CHIKUNGUNYA
Chikungunya IgG
Not specified
81148560003
Jun 22, 2015
CHIKUNGUNYA
Chikungunya IgG
EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
81148560003
Jun 22, 2015
CHIKUNGUNYA
CHICK IgG
Not specified
82532910026
Jan 02, 2023
CHIKUNGUNYA
CHICK IgG
DIA.PRO DIAGNOSTIC BIOPROBES SRL
82532910026
Jan 02, 2023
CHIKUNGUNYA
Chikungunya LF IgG IgM
ADVAGEN BIOTECH LTDA
81472060015
Sep 23, 2019
CHIKUNGUNYA
CHIKUNGUNYA VIRCLIA® IgM MONOTEST
VIRCELL S.L.
81816720081
Jan 27, 2025
CHIKUNGUNYA
CHIKUNGUNYA VIRCLIA® IgM MONOTEST
Not specified
81816720081
Jan 27, 2025
CHIKUNGUNYA
CHIKUNGUNYA VIRCLIA® IgG MONOTEST
VIRCELL S.L.
81816720080
Jan 06, 2025
CHIKUNGUNYA
CHIKUNGUNYA VIRCLIA® IgG MONOTEST
Not specified
81816720080
Jan 06, 2025
CHIKUNGUNYA
Família Controle Interno Chikungunya
programa nacional de controle de qualidade ltda
80155020043
Apr 15, 2024