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ANVISA registration 80391910019Active

Instrument for flow cytometry

ANVISA Registration Number: 80391910019PH 7 COMÉRCIO E REPRESENTAÇÕES DE PRODUTOS PARA DIAGNÓSTICOS LTDALUMINEX CORPORATIONRisk Class II
Verified
Device names
Technical name
Instrument for flow cytometry
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PT: Instrumento para citometria de fluxo
Commercial name
Instrumento FlexMap 3D
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Risk class
Class II
Registration details
Registration Number
80391910019
Process Number
25351031272202569
CNPJ
59920132000184
Company information
Registration Holder
PH 7 COMÉRCIO E REPRESENTAÇÕES DE PRODUTOS PARA DIAGNÓSTICOS LTDA
Manufacturer
LUMINEX CORPORATION
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Apr 28, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Instrument for flow cytometry in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80391910019 and manufactured by LUMINEX CORPORATION. The registration is held by PH 7 COMÉRCIO E REPRESENTAÇÕES DE PRODUTOS PARA DIAGNÓSTICOS 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.