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ANVISA registration 80686360130Active

Ultrasound Device

ANVISA Registration Number: 80686360130MANDALA 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 530 Compact
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Risk class
Class II
Registration details
Registration Number
80686360130
Process Number
25351036767201702
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
Mar 20, 2017
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 80686360130 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.