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Ophthalmic Refractometer - ANVISA Registration 80686679002

Access comprehensive regulatory information for Ophthalmic Refractometer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80686679002 and manufactured by VIEWLIGHT USA, LLC. The registration is held by EYEHOME COMÉRCIO DE PRODUTOS MÉDICOS 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 NIDEK CO., LTD (MAEHAMA), CARL ZEISS VISION GMBH, 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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80686679002
Registration Details
ANVISA Registration Number: 80686679002
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Device Details

REFRATOR MECÂNICO
Risk Class I

Registration Details

80686679002

25351356165201122

11972173000198

Company Information

VIEWLIGHT USA, LLC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jan 02, 2012

VIGENTE

09/18/2025 19:00:01