D-DIMER - ANVISA Registration 80105220185

Access comprehensive regulatory information for D-DIMER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80105220185 and manufactured by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA. The registration is held by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA with validity until Apr 15, 2034.

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 ROCHE DIAGNOSTICS GMBH, INSTRUMENTATION LABORATORY, 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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80105220185
Registration Details
ANVISA Registration Number: 80105220185
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FASTLINE D-DÍMERO
Risk Class III

Registration Details

80105220185

25351843566202374

04299232000143

Dates and Status

Apr 15, 2024

15/04/2034

09/18/2025 19:00:01