Laser System For Surgery - ANVISA Registration 80625080051

Access comprehensive regulatory information for Laser System For Surgery in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80625080051 and manufactured by NIDEK CO., LTD (MAEHAMA). The registration is held by NIDEK EYECARE DO BRASIL COMERCIO DE INSTRUMENTOS OPTICOS LTDA with validity until May 11, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including QUANTA SYSTEM SPA, DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS 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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80625080051
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Registration Details
ANVISA Registration Number: 80625080051
Janaina dos Santos de Miranda

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Related Devices (2)

SISTEMA DE YAG LASER OFTÁLMICO
Risk Class III

Registration Details

80625080051

25351352396202071

09632380000151

Company Information

Japan
PT: JAPÃO

Dates and Status

May 11, 2020

11/05/2030

09/18/2025 19:00:01

SISTEMA DE YAG LASER OFTÁLMICO
Risk Class III

Registration Details

80625080051

25351352396202071

09632380000151

Dates and Status

May 11, 2020

11/05/2030

09/18/2025 19:00:01