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ANVISA registration 80102513714Active

NEUROFILAMENTO DE CADEIA LEVE (NF-L)

ANVISA Registration Number: 80102513714VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDAFUJIREBIO EUROPE N.V.Risk Class II
Verified
Device names
Technical name
NEUROFILAMENTO DE CADEIA LEVE (NF-L)
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Commercial name
Familia Lumipulse G NfL
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Risk class
Class II
Registration details
Registration Number
80102513714
Process Number
25351125885202647
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
FUJIREBIO EUROPE N.V.
Manufacturing Country
Belgium
PT: BÉLGICA
Dates and status
Publication Date
Aug 17, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for NEUROFILAMENTO DE CADEIA LEVE (NF-L) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102513714 and manufactured by FUJIREBIO EUROPE N.V.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS 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.