GIARDIA LAMBLIA - ANVISA Registration 81249610021
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 81249610021 and manufactured by BIO BRASIL CIENCIA E TECNOLOGIA LTDA. The registration is held by BIO BRASIL CIENCIA E TECNOLOGIA 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
81249610021
25351856848202331
22213299000103
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
CORIS Bioconceptยฎ Giardia-Strip
Nanosens Ltda
81546350058
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

