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 81000030121

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 81000030121 and manufactured by MISONIX, INC. The registration is held by Autentica Medical Importação Comercio e Serviços LTDA-ME with validity until May 16, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including APYX MEDICAL CORPORATION, NEWPONG 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
81000030121
2 Related Devices
Registration Details
ANVISA Registration Number: 81000030121
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

ASPIRADOR CIRÚRGICO ULTRASSÔNICO neXus
Risk Class III

Registration Details

81000030121

25351459767202214

18192496000108

Company Information

MISONIX, INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 16, 2022

16/05/2032

09/18/2025 19:00:01

ASPIRADOR CIRÚRGICO ULTRASSÔNICO neXus
Risk Class III

Registration Details

81000030121

25351459767202214

18192496000108

Dates and Status

May 16, 2022

16/05/2032

09/18/2025 19:00:01