Laser System For Surgery - ANVISA Registration 80625080044

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 80625080044 and manufactured by NIDEK CO., LTD (MAEHAMA). The registration is held by NIDEK EYECARE DO BRASIL COMERCIO DE INSTRUMENTOS OPTICOS LTDA with validity until Apr 09, 2028.

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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80625080044
2 Related Devices
Registration Details
ANVISA Registration Number: 80625080044
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (2)

FOTOCOAGULADOR A LASER VERDE
Risk Class III

Registration Details

80625080044

25351130431201888

09632380000151

Company Information

Japan
PT: JAPÃO

Dates and Status

Apr 09, 2018

09/04/2028

09/18/2025 19:00:01

FOTOCOAGULADOR A LASER VERDE
Risk Class III

Registration Details

80625080044

25351130431201888

09632380000151

Dates and Status

Apr 09, 2018

09/04/2028

09/18/2025 19:00:01