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Collection Vials - ANVISA Registration 10306849023

Access comprehensive regulatory information for Collection Vials in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10306849023 and manufactured by GENADYNE BIOTECHNOLOGIES INC.. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA 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 3P MEDICAL LTDA, SEROPLAST INDÚSTRIA E COMÉRCIO DE PRODUTOS HOSPITALARES LTDA -ME, 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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10306849023
Registration Details
ANVISA Registration Number: 10306849023
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Device Details

Canister UNO Plus
Risk Class II

Registration Details

10306849023

25351609280202361

00028682000140

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 02, 2023

VIGENTE

09/18/2025 19:00:01