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

Applicators - ANVISA Registration 80003899016

Access comprehensive regulatory information for Applicators in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80003899016 and manufactured by BIOCER ENTWICKLUNGS GMBH. The registration is held by CANADA CENTRAL DE NEGOCIOS DO BRASIL 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 FAGA MEDICAL INDUSTRIA DE EQUIPAMENTOS E INSTRUMENTOS MEDICO-HOSPITALARES LTDA ME, Baxter Healthcare S.A., 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
80003899016
Registration Details
ANVISA Registration Number: 80003899016
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Aplicador Haemocer Flex
Risk Class II

Registration Details

80003899016

25351049134202536

01911022000176

Company Information

Germany
PT: ALEMANHA

Dates and Status

Apr 22, 2025

VIGENTE

09/18/2025 19:00:01