FOLATE - ANVISA Registration 10339840539
Access comprehensive regulatory information for FOLATE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10339840539 and manufactured by DIASORIN INC.. The registration is held by DIASORIN 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 ROCHE DIAGNOSTICS GMBH, ABBOTT IRELAND DIAGNOSTICS DIVISION, 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
10339840539
25351012189202248
01896764000170
Company Information
Dates and Status
Jun 09, 2022
VIGENTE
09/18/2025 19:00:01
ROCHE DIAGNOSTICS GMBHโข Germany
ABBOTT IRELAND DIAGNOSTICS DIVISIONโข Ireland
SIEMENS HEALTHCARE DIAGNOSTICS INCโข United States of America
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.โข China
TOSOH CORPORATIONโข Japan
FOLATO
Folate Reagent Kit
LABTEST DIAGNOSTICA S/A
10009010494
Jun 16, 2025
FOLATO
Familia MAGLUMI Folato (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102513423
May 12, 2025
FOLATO
Famรญlia Folate Chemiluminescent Binding Assay Kit
MACCURA BIOTECHNOLOGY CO LTD
82444370222
Apr 07, 2025
FOLATO
ID-Vitยฎ Folic acid in whole blood
IMMUNDIAGNOSTIK AG
80836930125
Jan 06, 2025
FOLATO
Folato Test System โ ELISA
MONOBIND, INC
80048490104
Dec 23, 2024

