GIARDIA LAMBLIA - ANVISA Registration 81546350058
Access comprehensive regulatory information for GIARDIA LAMBLIA in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81546350058 and manufactured by Nanosens Ltda. The registration is held by Nanosens 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, EPITOPE DIAGNOSTICS, INC., 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
81546350058
25351876356202362
25407581000101
Company Information
Dates and Status
Jan 15, 2024
VIGENTE
09/18/2025 19:00:01
R-BIOPHARM AGโข Germany
EPITOPE DIAGNOSTICS, INC.โข United States of America
ACRO BIOTECH, INC. (MONTCLAIR)โข United States of America
REMEL EUROPE LIMITEDโข United Kingdom
HANGZHOU BIOTEST BIOTECH CO., LTD,โข China
GIARDIA LAMBLIA
RIDASCREENยฎ Giardia
R-BIOPHARM AG
82890930004
Feb 17, 2025
GIARDIA LAMBLIA
Giardia lamblia - TF Quicktest
BIO BRASIL CIENCIA E TECNOLOGIA LTDA
81249610021
Jan 15, 2024
GIARDIA LAMBLIA
Cassete de Teste Rรกpido de Giardia lamblia (Fezes)
HANGZHOU ALLTEST BIOTECH CO. LTD
81325990253
Jun 05, 2023
GIARDIA LAMBLIA
FASTLINE GIARDIA LAMBLIA Ag
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA
80105220129
Apr 17, 2023
GIARDIA LAMBLIA
GIARDIA II
TECHLAB, INC
80001590005
Oct 20, 2022

