DIGITOXIN - ANVISA Registration 10287411251
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 10287411251 and manufactured by ROCHE DIAGNOSTICS GMBH. 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
10287411251
25351288806201783
30280358000186
Company Information
Dates and Status
Jul 31, 2017
23/06/2035
09/18/2025 19:00:01
DIGOXIN
Elecsys Digoxin
ROCHE DIAGNOSTICS GMBH
10287411250
Jul 31, 2017
DIGOXIN
Elecsys Digoxin
Not specified
10287411250
Jul 31, 2017
DIGOXIN
Elecsys Digoxina
Not specified
10287411135
Jun 27, 2016
DIGOXIN
Elecsys Digoxina
ROCHE DIAGNOSTICS GMBH
10287411135
Jun 27, 2016
DIGOXIN
ELECSYS CALSET DIGOXINA
ROCHE DIAGNOSTICS GMBH
10287410292
May 14, 2004