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Endoscopic Instruments - ANVISA Registration 82233960012

Access comprehensive regulatory information for Endoscopic Instruments in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82233960012 and manufactured by ARTHIMED INDUSTRIA E COMERCIO DE PRODUTOS MEDICOS HOSPITALARES LTDA. The registration is held by ARTHIMED INDUSTRIA E COMERCIO DE PRODUTOS MEDICOS 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, RZ MEDIZINTECHNIK GMBH, 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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82233960012
Registration Details
ANVISA Registration Number: 82233960012
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Device Details

FAMILIA DE INSTRUMENTAL ENDOSCÓPICO FLEXIVEL E SEMI RÍGIDO
Risk Class I

Registration Details

82233960012

25351133198202514

33745478000108

Dates and Status

Aug 11, 2025

VIGENTE

09/18/2025 19:00:01