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Graft Preparation System - ANVISA Registration 80894180001

Access comprehensive regulatory information for Graft Preparation System in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80894180001 and manufactured by Ipax, Inc. The registration is held by GID BRASIL COMERCIO E DISTRIBUIÇÃO DE PRODUTOS PARA A SAÚDE LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including HUMAN BRAIN WAVE SRL, NEXGEN IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MEDICOS E VETERINARIOS LTDA, 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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80894180001
2 Related Devices
Registration Details
ANVISA Registration Number: 80894180001
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Related Devices (2)

RECIPIENTE DE TECIDOS GID SVF-1
Risk Class II

Registration Details

80894180001

25351426238201304

15397121000196

Company Information

Ipax, Inc
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 14, 2014

VIGENTE

09/18/2025 19:00:01

RECIPIENTE DE TECIDOS GID SVF-1
Risk Class II

Registration Details

80894180001

25351426238201304

15397121000196

Company Information

The GID GROUP, Inc
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 14, 2014

VIGENTE

09/18/2025 19:00:01