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.
Related Devices (2)
Registration Details
10350530220
25351041271202107
01197835000146
Company Information
Dates and Status
Aug 30, 2021
30/08/2031
09/18/2025 19:00:01
COVIDIEN LLC• United States of America
STARMED CO., LTD.• South Korea
BOSTON SCIENTIFIC CORPORATION• United States of America
ARTHREX, INC.• United States of America
BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH• United States of America
EQUIPAMENTO DE RF PARA ABLAÇÃO
Gerador de Ablação por Eletroporação Irreversivel
ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD.
81504790382
Dec 04, 2023
EQUIPAMENTO DE RF PARA ABLAÇÃO
Gerador de Ablação por Eletroporação Irreversivel
Not specified
81504790382
Dec 04, 2023
EQUIPAMENTO DE RF PARA ABLAÇÃO
Gerador Barrx
Not specified
10349001306
May 29, 2023
EQUIPAMENTO DE RF PARA ABLAÇÃO
Gerador Barrx
COVIDIEN LLC
10349001306
May 29, 2023
EQUIPAMENTO DE RF PARA ABLAÇÃO
Sistema Rezum
Not specified
10341351009
Oct 24, 2022

