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

RF EQUIPMENT FOR ABLATION - ANVISA Registration 10350530220

Access comprehensive regulatory information for RF EQUIPMENT FOR ABLATION in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10350530220 and manufactured by STARMED CO., LTD.. The registration is held by LINE LIFE CARDIOVASCULAR COM DE PROD MED E HOSP LTDA with validity until Aug 30, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including COVIDIEN LLC, STARMED CO., LTD., 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
10350530220
2 Related Devices
Registration Details
ANVISA Registration Number: 10350530220
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

GERADOR VIVA MULTI RF
Risk Class III

Registration Details

10350530220

25351041271202107

01197835000146

Company Information

STARMED CO., LTD.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Aug 30, 2021

30/08/2031

09/18/2025 19:00:01

GERADOR VIVA MULTI RF
Risk Class III

Registration Details

10350530220

25351041271202107

01197835000146

Company Information

Dates and Status

Aug 30, 2021

30/08/2031

09/18/2025 19:00:01