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Instrument Kit - ANVISA Registration 80991380009

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80991380009 and manufactured by HELIOSCOPIE S. A.. The registration is held by DR IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including MARDEN MEDICAL LTDA, LIMA CORPORATE S.P.A, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80991380009
Registration Details
ANVISA Registration Number: 80991380009
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Device Details

Dispositivo para remoção do Balão Intragástrico Heliosphere
Risk Class II

Registration Details

80991380009

25351262906201711

17634786000100

Company Information

HELIOSCOPIE S. A.
France
PT: FRANÇA

Dates and Status

Jul 10, 2017

VIGENTE

09/18/2025 19:00:01