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Laser Device for Ophthalmological Treatment - ANVISA Registration 80170800018

Access comprehensive regulatory information for Laser Device for Ophthalmological Treatment in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80170800018 and manufactured by OPTOTEK D.O.O. The registration is held by OPTIVISION COMÉRCIO, IMPORTAÇÃO E EXPORTAÇÃO - LTDA - EPP with validity until Apr 22, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including CARL ZEISS MEDITEC AG, QUANTEL MEDICAL, 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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80170800018
2 Related Devices
Registration Details
ANVISA Registration Number: 80170800018
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Related Devices (2)

Equipamento de Terapia a Laser para Oftalmologia
Risk Class III

Registration Details

80170800018

25351857131202315

04601018000108

Company Information

OPTOTEK D.O.O
Slovenia
PT: ESLOVÊNIA

Dates and Status

Apr 22, 2024

22/04/2034

09/18/2025 19:00:01

Equipamento de Terapia a Laser para Oftalmologia
Risk Class III

Registration Details

80170800018

25351857131202315

04601018000108

Dates and Status

Apr 22, 2024

22/04/2034

09/18/2025 19:00:01