ENTAMOEBA SP - ANVISA Registration 80464810922
Access comprehensive regulatory information for ENTAMOEBA SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810922 and manufactured by HYSEN BIOTECH.LNC. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS 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 R-BIOPHARM AG, ACRO BIOTECH, INC. (MONTCLAIR), 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.
Device Details
Registration Details
80464810922
25351079361202596
09377976000152
Company Information
Dates and Status
Jun 16, 2025
VIGENTE
09/18/2025 19:00:01
R-BIOPHARM AG• Germany
ACRO BIOTECH, INC. (MONTCLAIR)• United States of America
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA• Brazil
REMEL EUROPE LIMITED• England (United Kingdom)
ACRO BIOTECH, INC• United States of America
ENTAMOEBA SP
RIDASCREEN® Entamoeba
R-BIOPHARM AG
82890930008
Apr 28, 2025
ENTAMOEBA SP
E. histolytica TF Quicktest
BIO BRASIL CIENCIA E TECNOLOGIA LTDA
81249610020
Jan 15, 2024
ENTAMOEBA SP
Família Cassete de Teste Rápido de Entamoeba histolytica (Fezes)
HANGZHOU ALLTEST BIOTECH CO., LTD
81325990289
Jul 31, 2023
ENTAMOEBA SP
FASTLINE ENTAMOEBA HISTOLYTICA Ag
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA
80105220121
Mar 13, 2023
ENTAMOEBA SP
E. HISTOLYTICA II
TECHLAB, INC
80001590004
Oct 13, 2022

