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Reinfusion Bag - ANVISA Registration 81118639007

Access comprehensive regulatory information for Reinfusion Bag in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81118639007 and manufactured by BIMINI HEALTH TECH. The registration is held by OPTME IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS LTDA – ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including Puregraft LLC, STRYKER MEDICAL, 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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81118639007
Registration Details
ANVISA Registration Number: 81118639007
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Device Details

PureGraft 250/850 System
Risk Class II

Registration Details

81118639007

25351445891202375

19739452000118

Company Information

BIMINI HEALTH TECH
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 24, 2023

VIGENTE

09/18/2025 19:00:01