PREGNENOLONE - ANVISA Registration 80836930103
Access comprehensive regulatory information for PREGNENOLONE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80836930103 and manufactured by LDN- LABOR DIAGNOSTIKA NORD GMBH & CO, KG. The registration is held by ARBO DISTRIBUIDORA DE PRODUTOS PARA LABORATรRIOS 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 LDN LABOR DIAGNOSTIKA NORD GMBH & CO., IMMUNDIAGNOSTIK AG, 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
80836930103
25351068025202356
06203702000159
Company Information
Dates and Status
Feb 27, 2023
VIGENTE
09/18/2025 19:00:01
LDN LABOR DIAGNOSTIKA NORD GMBH & CO.โข Germany
IMMUNDIAGNOSTIK AGโข Germany
DIAGNOSTICS BIOCHEM CANADA INCโข Canada
EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDAโข Brazil
EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AGโข Germany
PREGNENOLONA
Pregnenolona ELISA
EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
10338930255
Aug 19, 2021
PREGNENOLONA
PREGNENOLONA
DIAGNOSTICS BIOCHEM CANADA INC
10300390496
May 20, 2019
PREGNENOLONA
Pregnenolona
EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA
10338930215
Mar 18, 2019
PREGNENOLONA
PREGNENOLONE ELISA
LDN LABOR DIAGNOSTIKA NORD GMBH & CO.
80464810591
Jul 30, 2018
PREGNENOLONA
Pregnenolone sulfate LC-MS/MS Kit
IMMUNDIAGNOSTIK AG
80464810576
Jul 02, 2018

