ANVISA registration 80583400036Valid until Aug 03, 2036INTRACRANIAL VASCULAR STENT
ANVISA Registration Number: 80583400036ENDOTEC PRODUTOS MEDICOS S/AMICROVENTION EUROPE SARLRisk Class IV
Device names
- Technical name
- INTRACRANIAL VASCULAR STENT
- Commercial name
- STENT FRED X 2.5/3.0 - DISPOSITIVO ENDOLUMINAL DE REDIRECIONAMENTO DE FLUXO
- Risk class
- Class IV
PT: STENT VASCULAR INTRACRANIANO
Registration details
- Registration Number
- 80583400036
- Process Number
- 25351229594202465
- CNPJ
- 09586279000101
Company information
- Registration Holder
- ENDOTEC PRODUTOS MEDICOS S/A
- Manufacturer
- MICROVENTION EUROPE SARL
- Manufacturing Country
- France
PT: FRANÇA
Dates and status
- Publication Date
- Aug 03, 2026
- Validity
- 03/08/2036
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for INTRACRANIAL VASCULAR STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80583400036 and manufactured by MICROVENTION EUROPE SARL. The registration is held by ENDOTEC PRODUTOS MEDICOS S/A with validity until Aug 03, 2036.
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