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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
80625080051
25351352396202071
09632380000151
Company Information
Dates and Status
May 11, 2020
11/05/2030
09/18/2025 19:00:01
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