Pure Global

Articles and Materials For In Vitro Fertilization - ANVISA Registration 83085839007

Access comprehensive regulatory information for Articles and Materials For In Vitro Fertilization in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 83085839007 and manufactured by VITROLIFE SWEDEN AB. The registration is held by VITROLIFE BRASIL COMERCIO DE EQUIPAMENTOS LABORATORIAIS 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 VITROLIFE SWEDEN AB, ALLWIN MEDICAL DEVICES, INC, 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
83085839007
Registration Details
ANVISA Registration Number: 83085839007
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Conjunto de Aspiração Folicular - Lúmen Único com Luer
Risk Class II

Registration Details

83085839007

25351140608202583

54416180000116

Company Information

Sweden
PT: SUÉCIA

Dates and Status

Aug 18, 2025

VIGENTE

09/18/2025 19:00:01