RF EQUIPMENT FOR ABLATION - ANVISA Registration 80804050281
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 80804050281 and manufactured by ARTHROCARE CORPORATION. The registration is held by Smith & Nephew Comércio de Produtos Médicos Ltda. with validity until Jan 20, 2030.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including STARMED CO., LTD., COVIDIEN 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.
Related Devices (2)
Registration Details
80804050281
25351711503201973
13656820000188
Company Information
Dates and Status
Jan 20, 2020
20/01/2030
09/18/2025 19:00:01
STARMED CO., LTD.• South Korea
COVIDIEN LLC• United States of America
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

