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ANTICARDIOLIPIN - ANVISA Registration 80003610599

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 80003610599 and manufactured by INSTRUMENTATION LABORATORY CO.. The registration is held by WERFEN MEDICAL 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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80003610599
Registration Details
ANVISA Registration Number: 80003610599
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Device Details

Famรญlia HemosIL AcuStar Anti-Cardiolipin IgM
Risk Class II

Registration Details

80003610599

25351644065202064

02004662000165

Company Information

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

Dates and Status

Dec 17, 2020

VIGENTE

09/18/2025 19:00:01