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Headlight - ANVISA Registration 80070210019

Access comprehensive regulatory information for Headlight in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80070210019 and manufactured by ZUMAX MEDICAL CO, LTD.. The registration is held by COMERCIO DE MATERIAIS MEDICOS HOSPITALARES MACROSUL 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 QED INC., MIKATOS INDUSTRIA, COMERCIO, SERVICOS E IMPORTACAO - LTDA - EPP, 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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80070210019
Registration Details
ANVISA Registration Number: 80070210019
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Device Details

FOTÓFORO MD
Risk Class I

Registration Details

80070210019

25351189231201181

95433397000111

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 13, 2011

VIGENTE

09/18/2025 19:00:01