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LASER SYSTEM KIT FOR SURGERY - ANVISA Registration 80102512361

Access comprehensive regulatory information for LASER SYSTEM KIT 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 80102512361 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS Mร‰DICOS LTDA with validity until Nov 25, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ANGIODYNAMICS, INC, AMO MANUFACTURING USA, LLC, 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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80102512361
2 Related Devices
Registration Details
ANVISA Registration Number: 80102512361
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Related Devices (2)

Kit de Procedimento VenaCure EVLT NeverTouch โ€“ FRS
Risk Class III

Registration Details

80102512361

25351479502201929

04718143000194

Dates and Status

Nov 25, 2019

25/11/2029

09/18/2025 19:00:01

Kit de Procedimento VenaCure EVLT NeverTouch โ€“ FRS
Risk Class III

Registration Details

80102512361

25351479502201929

04718143000194

Company Information

ANGIODYNAMICS, INC
United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Nov 25, 2019

25/11/2029

09/18/2025 19:00:01