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Headlight - ANVISA Registration 80070210092

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 80070210092 and manufactured by BISTOS 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., ZUMAX MEDICAL 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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80070210092
Registration Details
ANVISA Registration Number: 80070210092
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Device Details

Fotóforo LED para Exames Clínicos Omni MD
Risk Class I

Registration Details

80070210092

25351540762202217

95433397000111

Company Information

BISTOS CO., LTD
South Korea
PT: CORÉIA DO SUL

Dates and Status

May 26, 2022

VIGENTE

09/18/2025 19:00:01