ANDROSTENEDIONE - ANVISA Registration 10287411605
Access comprehensive regulatory information for ANDROSTENEDIONE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10287411605 and manufactured by ROCHE DIAGNOSTICS GMBH. The registration is held by ROCHE DIAGNÓSTICA BRASIL 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 DIAMETRA S.R.L., SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED, 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
10287411605
25351121517202204
30280358000186
Company Information
Dates and Status
Jul 07, 2022
VIGENTE
09/18/2025 19:00:01
ANDROSTENEDIONA
Família MAGLUMI Androstenedione (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102513517
Sep 15, 2025
ANDROSTENEDIONA
Família MAGLUMI Androstenediona (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102512905
Nov 21, 2022
ANDROSTENEDIONA
Androstenediona ELISA
EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
10338930268
Sep 09, 2021
ANDROSTENEDIONA
Família Elecsys Androstenedione
ROCHE DIAGNOSTICS GMBH
10287411569
May 13, 2021
ANDROSTENEDIONA
Atellica IM Androstenediona (ANDRO)
SIEMENS HEALTHCARE DIAGNOSTICS INC.
10345162377
Aug 17, 2020

