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

Morcellators - ANVISA Registration 81070509006

Access comprehensive regulatory information for Morcellators in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81070509006 and manufactured by SIMAI CO., LTD.. The registration is held by ALLENT COMERCIO, IMPORTACAO E DISTRIBUICAO DE MATERIAIS MEDICOS LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including VEOL MEDICAL TECHNOLOGIES PVT. LTD., TECNOCIRURGICA COMERCIO DE MATERIAIS MEDICOS CIRURGICOS E HOSPITALARES LTDA, 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
81070509006
Registration Details
ANVISA Registration Number: 81070509006
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Sistema Morcelador Genius SPS600
Risk Class II

Registration Details

81070509006

25351961257202466

17781132000109

Company Information

SIMAI CO., LTD.
China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

Apr 01, 2024

VIGENTE

09/18/2025 19:00:01