Guide - ANVISA Registration 80081350037

Access comprehensive regulatory information for Guide in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80081350037 and manufactured by CIRCON ACMI CORP. 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 similar products found using AI-powered semantic search, 5 companies making the same product including DPS INDUSTRIA, DISTRIBUICAO, COMERCIO, IMPORTACAO E EXPORTACAO LTDA, CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA., 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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80081350037
Registration Details
ANVISA Registration Number: 80081350037
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

GUIA URETERAIS CIRCON ACMI
Risk Class II

Registration Details

80081350037

25351017909200307

02620178000160

Company Information

CIRCON ACMI CORP
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 16, 2003

VIGENTE

09/18/2025 19:00:01