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ANVISA registration 80102511753Active

FIBRINOGEN

ANVISA Registration Number: 80102511753VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDADIAGNOSTICA STAGO S.A.S.Risk Class II
Verified
Device names
Technical name
FIBRINOGEN
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PT: FIBRINOGÊNIO
Commercial name
FAMÍLIA STA® LIATEST® FM
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Risk class
Class II
Registration details
Registration Number
80102511753
Process Number
25351891986201650
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
DIAGNOSTICA STAGO S.A.S.
Manufacturing Country
France
PT: FRANÇA
Dates and status
Publication Date
Jan 30, 2017
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for FIBRINOGEN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102511753 and manufactured by DIAGNOSTICA STAGO S.A.S.. 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.