Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Laser System For Surgery - ANVISA Registration 10341351004

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 10341351004 and manufactured by LUMENIS LIMITED. The registration is held by BOSTON SCIENTIFIC DO BRASIL LTDA with validity until Jul 16, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including QUANTA SYSTEM SPA, NIDEK CO., LTD (MAEHAMA), 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 Competitors
5 Recent Registrations
10341351004
2 Related Devices
Registration Details
ANVISA Registration Number: 10341351004
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

EQUIPAMENTO A LASER PARA TERAPIA
Risk Class III

Registration Details

10341351004

25351523646202225

01513946000114

Company Information

LUMENIS LIMITED
Israel
PT: ISRAEL

Dates and Status

May 16, 2022

16/07/2027

09/18/2025 19:00:01

EQUIPAMENTO A LASER PARA TERAPIA
Risk Class III

Registration Details

10341351004

25351523646202225

01513946000114

Company Information

Dates and Status

May 16, 2022

16/07/2027

09/18/2025 19:00:01