Materials for Endotoxin Detection - ANVISA Registration 80022060101

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 80022060101 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 similar products found using AI-powered semantic search, 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.

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80022060101
Registration Details
ANVISA Registration Number: 80022060101
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

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

Registration Details

80022060101

25351223588201937

60397874000156

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 08, 2019

VIGENTE

09/18/2025 19:00:01