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ANVISA registration 82910510005Active

Instrument intended for immunoassays

ANVISA Registration Number: 82910510005NACH BRASIL PRODUTOS DIAGNOSTICOS LTDAAESKU DIAGNOSTICS GMBH & CO. KGRisk Class II
Verified
Device names
Technical name
Instrument intended for immunoassays
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PT: Instrumento destinado a imunoensaios
Commercial name
HELIOS® AUTOMATED IFA SYSTEM
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Risk class
Class II
Registration details
Registration Number
82910510005
Process Number
25351134033202560
CNPJ
50161001000196
Company information
Registration Holder
NACH BRASIL PRODUTOS DIAGNOSTICOS LTDA
Manufacturer
AESKU DIAGNOSTICS GMBH & CO. KG
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Sep 15, 2025
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for Instrument intended for immunoassays in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82910510005 and manufactured by AESKU DIAGNOSTICS GMBH & CO. KG. The registration is held by NACH BRASIL PRODUTOS DIAGNOSTICOS 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.