Graft Preparation System - ANVISA Registration 80023450063

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 80023450063 and manufactured by ZIMMER SURGICAL, INC. The registration is held by TELLUS COMERCIO IMPORTAÇÃO E EXPORTAÇÃO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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80023450063
Registration Details
ANVISA Registration Number: 80023450063
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

EXPANSOR DE ENXERTO DE PELE SKINGRAFT MESHER ZIMMER TM
Risk Class II

Registration Details

80023450063

25351505428200699

01021137000195

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 12, 2007

VIGENTE

09/18/2025 19:00:01