Cutter - ANVISA Registration 81000030101

Access comprehensive regulatory information for Cutter in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81000030101 and manufactured by Misonix Incorporated. The registration is held by Autentica Medical Importação Comercio e Serviços LTDA-ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ABBOTT MEDICAL, NOVATECH SCIENTIFIC, 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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81000030101
Registration Details
ANVISA Registration Number: 81000030101
Janaina dos Santos de Miranda

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Device Details

CORTADOR DE OSSO ULTRASÔNICO MISONIX BONESCALPEL
Risk Class II

Registration Details

81000030101

25351358087202012

18192496000108

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 15, 2020

VIGENTE

09/18/2025 19:00:01