FECAL PARASITOLOGICAL TEST (KATO-KATZ) - ANVISA Registration 81064970002
Access comprehensive regulatory information for FECAL PARASITOLOGICAL TEST (KATO-KATZ) in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81064970002 and manufactured by ANA PAULA RUMAN ME. The registration is held by ANA PAULA RUMAN ME with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including EPITOPE DIAGNOSTICS, BIO BRASIL BIOTECNOLOGIA LTDA, and 3 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.
Device Details
Registration Details
81064970002
25351115270201983
11614477000183
Company Information
Dates and Status
Apr 08, 2019
VIGENTE
09/18/2025 19:00:01
PARASITOLÓGICO DE FEZES (KATO-KATZ)
Fecal Ova/Parasite Concentration Kit
EPITOPE DIAGNOSTICS
80464810596
Aug 27, 2018
PARASITOLÓGICO DE FEZES (KATO-KATZ)
HELM TESTE BIO - MANGUINHOS
FUNDAÇÃO OSWALDO CRUZ
80142170028
Mar 11, 2013
PARASITOLÓGICO DE FEZES (KATO-KATZ)
TF-TEST
BIO BRASIL BIOTECNOLOGIA LTDA
80680420001
Nov 07, 2011

