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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.

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80804050281
2 Related Devices
Registration Details
ANVISA Registration Number: 80804050281
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Related Devices (2)

Sistema Coblator II (RF8000E)
Risk Class III

Registration Details

80804050281

25351711503201973

13656820000188

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jan 20, 2020

20/01/2030

09/18/2025 19:00:01

Sistema Coblator II (RF8000E)
Risk Class III

Registration Details

80804050281

25351711503201973

13656820000188

Company Information

Dates and Status

Jan 20, 2020

20/01/2030

09/18/2025 19:00:01