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

Electrosurgical system - ANVISA Registration 80302210046

Access comprehensive regulatory information for Electrosurgical system in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80302210046 and manufactured by APYX MEDICAL CORPORATION. The registration is held by MINAS IMPORT LTDA with validity until Apr 06, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including NEWPONG 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80302210046
2 Related Devices
Registration Details
ANVISA Registration Number: 80302210046
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Gerador Eletrobisturi de alta frequência Bovie/Renuvion Ultimate 2
Risk Class III

Registration Details

80302210046

25351139733201901

00279767000100

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 06, 2020

06/04/2030

09/18/2025 19:00:01

Gerador Eletrobisturi de alta frequência Bovie/Renuvion Ultimate 2
Risk Class III

Registration Details

80302210046

25351139733201901

00279767000100

Company Information

Dates and Status

Apr 06, 2020

06/04/2030

09/18/2025 19:00:01