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ANVISA registration 80686369019Active

Ultrasound Device

ANVISA Registration Number: 80686369019MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDAECHOSENSRisk Class II
Verified
Device names
Technical name
Ultrasound Device
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PT: Aparelho de Ultra-Som
Commercial name
FibroScan 630
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Risk class
Class II
Registration details
Registration Number
80686369019
Process Number
25351506973202131
CNPJ
09117476000181
Company information
Registration Holder
MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDA
Manufacturer
ECHOSENS
Manufacturing Country
France
PT: FRANÇA
Dates and status
Publication Date
May 27, 2021
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Ultrasound Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80686369019 and manufactured by ECHOSENS. The registration is held by MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR 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.