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ANTICARDIOLIPIN - ANVISA Registration 10280220197

Access comprehensive regulatory information for ANTICARDIOLIPIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10280220197 and manufactured by HEMAGEN DIAGNOSTICS INC.. The registration is held by HEMAGEN DIAGNOSTICOS COMERCIO IMP E EXPORTACAO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ORGENTEC DIAGNOSTIKA GMBH, PHADIA AB, 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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10280220197
Registration Details
ANVISA Registration Number: 10280220197
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Device Details

Anticardiolipina GM- ELISA-Kit Jumbo
Risk Class II

Registration Details

10280220197

25351855594200864

64002686000132

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Nov 22, 2010

VIGENTE

09/18/2025 19:00:01