ANVISA registration 80102511751ActiveFIBRINOGEN/FIBRIN DEGRADATION PRODUCT (FDP)
ANVISA Registration Number: 80102511751VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDADIAGNOSTICA STAGO S.A.S.Risk Class II
Device names
- Technical name
- FIBRINOGEN/FIBRIN DEGRADATION PRODUCT (FDP)
- Risk class
- Class II
PT: PRODUTO DE DEGRADAÇÃO DE FIBRINOGÊNIO/ FIBRINA (FDP)
Registration details
- Registration Number
- 80102511751
- Process Number
- 25351891945201653
- 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/FIBRIN DEGRADATION PRODUCT (FDP) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102511751 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).
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