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Applicators - ANVISA Registration 81966280003

Access comprehensive regulatory information for Applicators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81966280003 and manufactured by MEDMIX SWITZERLAND AG. The registration is held by GEKA DO BRASIL INDUSTRIA E COMERCIO DE EMBALAGENS 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 FAGA MEDICAL INDUSTRIA DE EQUIPAMENTOS E INSTRUMENTOS MEDICO-HOSPITALARES LTDA ME, Baxter Healthcare S.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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81966280003
Registration Details
ANVISA Registration Number: 81966280003
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Device Details

Dispensador MIXPAC
Risk Class I

Registration Details

81966280003

25351381875202002

20434492000130

Company Information

Switzerland
PT: SUรร‡A

Dates and Status

May 14, 2020

VIGENTE

09/18/2025 19:00:01