ANVISA registration 80899119006Active

Sistema de discectomia, percutâneo, automático

Name: Sistema de discectomia, percutâneo, automático — ANVISA registration 80899119006
Creator: ADRIA S.R.L.
Keywords: Sistema de discectomia, percutâneo, automático, KIT CÂNULA HERNIATOME, 80899119006, Risk Class II, ANVISA registration

ANVISA Registration Number: 80899119006BIOIMPORTS COMERCIO IMPORTACAO, EXPORTACAO DE PRODUTOS MEDICOS LTDAADRIA S.R.L.Risk Class II

Verified

Device names

Technical name: Sistema de discectomia, percutâneo, automático
Commercial name: KIT CÂNULA HERNIATOME
Risk class: Class II

Registration details

Registration Number: 80899119006
Process Number: 25351113279202255
CNPJ: 10729586000183

Company information

Registration Holder: BIOIMPORTS COMERCIO IMPORTACAO, EXPORTACAO DE PRODUTOS MEDICOS LTDA
Manufacturer: ADRIA S.R.L.
Manufacturing Country: Italy

Dates and status

Publication Date: Jun 23, 2022
Validity: VIGENTE
Last Updated: 08/18/2026 19:00:00

About this record

Access comprehensive regulatory information for Sistema de discectomia, percutâneo, automático in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80899119006 and manufactured by ADRIA S.R.L.. The registration is held by BIOIMPORTS COMERCIO IMPORTACAO, EXPORTACAO DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

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