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Guide - ANVISA Registration 10275169007

Access comprehensive regulatory information for Guide in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10275169007 and manufactured by SAFEWIRE LLC. The registration is held by SUPORTE HOSPITALAR 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 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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10275169007
Registration Details
ANVISA Registration Number: 10275169007
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Device Details

FUNNEL
Risk Class I

Registration Details

10275169007

25351077841201316

73857393000128

Company Information

SAFEWIRE LLC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 03, 2013

VIGENTE

09/18/2025 19:00:01