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Instrument Kit - ANVISA Registration 81050760116

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81050760116 and manufactured by NOVAX DMA S.A. The registration is held by GUSMED DO BRASIL COMERCIO E LOCAร‡รƒO DE PRODUTOS MEDICOS LTDA - EPP 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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81050760116
Registration Details
ANVISA Registration Number: 81050760116
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Device Details

Kit Instrumental Distrator MISS Lateral
Risk Class I

Registration Details

81050760116

25351958127202012

19443457000107

Company Information

NOVAX DMA S.A
Argentina
PT: ARGENTINA

Dates and Status

Sep 17, 2020

VIGENTE

09/18/2025 19:00:01