CARCINOEMBRYONIC ANTIGEN - ANVISA Registration 81325990183

Access comprehensive regulatory information for CARCINOEMBRYONIC ANTIGEN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81325990183 and manufactured by manufacturer not specified. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until May 17, 2031.

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 ABBOTT IRELAND DIAGNOSTIC DIVISION, ROCHE DIAGNOSTICS GMBH, 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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81325990183
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Registration Details
ANVISA Registration Number: 81325990183
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Cassete de Teste para CEA (soro/plasma)
Risk Class III

Registration Details

81325990183

25351254440202169

19933144000129

Dates and Status

May 17, 2021

17/05/2031

09/18/2025 19:00:01

Família Cassete de Teste para CEA (soro/plasma)
Risk Class III

Registration Details

81325990183

25351254440202169

19933144000129

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 17, 2021

17/05/2031

09/18/2025 19:00:01