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

Materials for Endotoxin Detection - ANVISA Registration 80022060098

Access comprehensive regulatory information for Materials for Endotoxin Detection in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80022060098 and manufactured by FUJIFILM WAKO CHEMICALS U.S.A. CORPORATION. The registration is held by FUJIFILM 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 LONZA WALKERSVILLE, INC., FUJIFILM WAKO PURE CHEMICAL CORPORATION, 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
80022060098
Registration Details
ANVISA Registration Number: 80022060098
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

PYROSTAR™ ES-F Multi Teste Lisado com CSE Correspondente
Risk Class II

Registration Details

80022060098

25351223585201901

60397874000156

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 01, 2019

VIGENTE

09/18/2025 19:00:01