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

Blood Administration Set - ANVISA Registration 80463919020

Access comprehensive regulatory information for Blood Administration Set in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80463919020 and manufactured by FORTECARE INDÚSTRIA DE PRODUTOS MÉDICOS LTDA. The registration is held by FORTECARE INDÚSTRIA DE PRODUTOS MÉDICOS 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 LIFEMED INDUSTRIAL DE EQUIPAMENTOS E ARTiGOS MÉDICOS E HOSPITALARES S.A, FORTECARE INDÚSTRIA DE PRODUTOS MÉDICOS 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
80463919020
Registration Details
ANVISA Registration Number: 80463919020
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

LINHA SANGUÍNEA VENOSA PARA HEMODIÁLISE
Risk Class II

Registration Details

80463919020

25351364318202361

08474646000112

Company Information

Brazil
PT: BRASIL

Dates and Status

Jun 26, 2023

VIGENTE

09/18/2025 19:00:01