C-REACTIVE PROTEIN - ANVISA Registration 10009010198
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 10009010198 and manufactured by LABTEST DIAGNOSTICA S/A. The registration is held by LABTEST DIAGNOSTICA S/A 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, KOVALENT DO BRASIL 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.

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Registration Details
10009010198
25351005067201171
16516296000138
Company Information
Dates and Status
Feb 22, 2011
VIGENTE
09/18/2025 19:00:01
C-REACTIVE PROTEIN
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10159820056
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10377390236
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ULTRASENSITIVE C-REACTIVE PROTEIN
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LABTEST DIAGNOSTICA S/A
10009010208
Mar 21, 2011
C-REACTIVE PROTEIN
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Sep 21, 2020
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82444370250
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VIDAturbi PCR
Vida Biotecnologia Ltda - ME
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
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