C-REACTIVE PROTEIN - ANVISA Registration 80254180412
Access comprehensive regulatory information for C-REACTIVE PROTEIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80254180412 and manufactured by THERMO FISHER SCIENTIFIC OY. 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, 5 similar products found using AI-powered semantic search, 5 companies making the same product including Nanosens Ltda, LABTEST DIAGNOSTICA S/A, 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.

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Registration Details
80254180412
25351272757202268
04930429000139
Company Information
Dates and Status
Apr 20, 2022
VIGENTE
09/18/2025 19:00:01
C-REACTIVE PROTEIN
Família CRP
ROCHE DIAGNOSTICS GMBH
10287411499
Jun 15, 2020
C-REACTIVE PROTEIN
FAMÍLIA PROTEÍNA C REATIVA
QUIBASA QUÍMICA BÁSICA LTDA
10269360368
Nov 21, 2022
C-REACTIVE PROTEIN
Família AFIAS CRP
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10350840337
Oct 15, 2018
C-REACTIVE PROTEIN
Família ichroma CRP
BODITECH MED INC.
10350840286
Oct 03, 2016
C-REACTIVE PROTEIN
FAMÍLIA PROTEINA C-REATIVA (PCR)
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80367750160
Nov 21, 2022
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82533950117
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82444370250
Jun 16, 2025
PROTEÍNA C REATIVA
VIDAturbi PCR
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80785070266
Apr 28, 2025
PROTEÍNA C REATIVA
Família PCR Turbi
KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO LTDA
10377390293
Mar 05, 2025
PROTEÍNA C REATIVA
LumiraDx CRP Test
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10287411736
Mar 05, 2025