THEOPHYLLINE - ANVISA Registration 80254180409

Access comprehensive regulatory information for THEOPHYLLINE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180409 and manufactured by MICROGENICS CORPORATION. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Apr 18, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including ROCHE DIAGNOSTICS GMBH, ORTHO CLINICAL DIAGNOSTICS, INC, 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.

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80254180409
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Registration Details
ANVISA Registration Number: 80254180409
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

CEDIA Theophylline II Assay
Risk Class III

Registration Details

80254180409

25351053052202243

04930429000139

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 18, 2022

18/04/2032

09/18/2025 19:00:01

CEDIA Theophylline II Assay
Risk Class III

Registration Details

80254180409

25351053052202243

04930429000139

Company Information

Dates and Status

Apr 18, 2022

18/04/2032

09/18/2025 19:00:01

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