DIGITOXIN - ANVISA Registration 10287411315
Access comprehensive regulatory information for DIGITOXIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10287411315 and manufactured by manufacturer not specified. The registration is held by ROCHE DIAGNÓSTICA BRASIL LTDA with validity until Jun 23, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including ROCHE DIAGNOSTICS GMBH, and 2 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
10287411315
25351691929201731
30280358000186
Company Information
Dates and Status
Mar 19, 2018
23/06/2035
09/18/2025 19:00:01
DIGOXIN - CLASS II
DIGOXIN
BECKMAN COULTER IRELAND INC.
10033120811
Sep 16, 2013
DIGOXIN - CLASS II
DIGOXIN
BECKMAN COULTER, INC.
10033120811
Sep 16, 2013
DIGOXIN - CLASS II
DIGOXINA
ROCHE DIAGNOSTICS GMBH
10287410647
Jul 23, 2007
CYCLOSPORINE
Cyclosporine Calset
ROCHE DIAGNOSTICS GMBH
10287411028
Dec 02, 2013
CYCLOSPORINE
Cyclosporine Calset
Not specified
10287411028
Dec 02, 2013