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ANVISA registration 10338930304Active

ANTINUCLEAR ANTIBODY (ANA)

ANVISA Registration Number: 10338930304EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDAEUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDARisk Class II
Verified
Device names
Technical name
ANTINUCLEAR ANTIBODY (ANA)
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PT: ANTICORPO ANTINUCLEAR (ANA)
Commercial name
IIFT: Crithidia luciliae (anti-dsDNA)
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Risk class
Class II
Registration details
Registration Number
10338930304
Process Number
25351840065202336
CNPJ
93741726000166
Company information
Registration Holder
EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA
Manufacturer
EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Jan 02, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for ANTINUCLEAR ANTIBODY (ANA) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10338930304 and manufactured by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.