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ANVISA registration 80303610020Active

HOLTER SYSTEM AND NON-INVASIVE BLOOD PRESSURE MONITOR

ANVISA Registration Number: 80303610020AURION EQUIPAMENTOS ELETRÔNICOS LTDA -MEMEDITECH KFTRisk Class II
Verified
Device names
Technical name
HOLTER SYSTEM AND NON-INVASIVE BLOOD PRESSURE MONITOR
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PT: SISTEMA HOLTER E MONITOR DE PRESSÃO ARTERIAL NÃO-INVASIVO
Commercial name
CARD(x)PLORE
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Risk class
Class II
Registration details
Registration Number
80303610020
Process Number
25351656186200862
CNPJ
06889652000105
Company information
Registration Holder
AURION EQUIPAMENTOS ELETRÔNICOS LTDA -ME
Manufacturer
MEDITECH KFT
Manufacturing Country
Hungary
PT: HUNGRIA
Dates and status
Publication Date
May 25, 2009
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for HOLTER SYSTEM AND NON-INVASIVE BLOOD PRESSURE MONITOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80303610020 and manufactured by MEDITECH KFT. The registration is held by AURION EQUIPAMENTOS ELETRÔNICOS LTDA -ME 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.