DIGOXIN - ANVISA Registration 10287411422
Access comprehensive regulatory information for DIGOXIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10287411422 and manufactured by manufacturer not specified. The registration is held by ROCHE DIAGNÓSTICA BRASIL LTDA with validity until Jul 21, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 4 companies making the same product including ROCHE DIAGNOSTICS GMBH, MICROGENICS CORPORATION, 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.
Related Devices (2)
Registration Details
10287411422
25351208839201901
30280358000186
Company Information
Dates and Status
Jul 29, 2019
21/07/2035
09/18/2025 19:00:01
DIGOXINA
Família MAGLUMI Digoxina (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102513357
Jan 20, 2025
DIGOXINA
Família MAGLUMI Digoxina (CLIA)
Not specified
80102513357
Jan 20, 2025
DIGOXINA
DRI Digoxin Assay
Not specified
80254180467
Sep 02, 2024
DIGOXINA
DRI Digoxin Assay
MICROGENICS CORPORATION
80254180467
Sep 02, 2024
DIGOXINA
REATIVO SECO VITROS* PARA DIGOXINA DGXN
Not specified
81246986728
Aug 28, 2017

