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Instrument Kit - ANVISA Registration 81050769013

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 81050769013 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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81050769013
Registration Details
ANVISA Registration Number: 81050769013
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Device Details

Kit para Injeรงรฃo de Cimento em Parafuso Pedicular Fenestrado Novax DMA
Risk Class II

Registration Details

81050769013

25351160561202141

19443457000107

Company Information

NOVAX DMA S.A
Argentina
PT: ARGENTINA

Dates and Status

Sep 02, 2021

VIGENTE

09/18/2025 19:00:01