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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Registration Details
80081350037
25351017909200307
02620178000160
Company Information
Dates and Status
Sep 16, 2003
VIGENTE
09/18/2025 19:00:01
Guide Wire
GUIA URETERAL GTA
GTA SRL
80438830001
Sep 22, 2014
Guide Wire
GUIA URETERAL GTA
GTA SRL
10315990072
Nov 30, 2010
GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR
FIO GUIA UROLÓGICO REVESTIDO EM PTFE
LAKE REGION MEDICAL LIMITED
10341350737
Sep 16, 2013
GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR
FIO GUIA UROLÓGICO REVESTIDO EM PTFE
LAKE REGION MEDICAL
10341350737
Sep 16, 2013
Guide Wire
FIO GUIA PARA USO UROLÓGICO
UROVISION GMBH
80073110097
Feb 19, 2018
DPS INDUSTRIA, DISTRIBUICAO, COMERCIO, IMPORTACAO E EXPORTACAO LTDA• Brazil
CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA.• Brazil
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ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD.• China
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