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Accessories For Endoscopy - ANVISA Registration 80081350377

Access comprehensive regulatory information for Accessories For Endoscopy in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80081350377 and manufactured by GYRUS ACMI INC.. The registration is held by FLEX LAB COMERCIO DE MATERIAIS CIRURGICOS E 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 FUJIFILM CORPORATION, CHANGZHOU HEALTH MICROPORT MEDICAL DEVICES CO.,LTD, 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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80081350377
Registration Details
ANVISA Registration Number: 80081350377
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Device Details

Registration Details

80081350377

25351266189201248

02620178000160

Company Information

GYRUS ACMI INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 20, 2013

VIGENTE

09/18/2025 19:00:01