THEOPHYLLINE - ANVISA Registration 81246986783

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 81246986783 and manufactured by ORTHO CLINICAL DIAGNOSTICS, INC. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until Feb 24, 2035.

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, 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.

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81246986783
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Registration Details
ANVISA Registration Number: 81246986783
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

REATIVO SECO VITROS* PARA TEOFILINA THEO
Risk Class III

Registration Details

81246986783

25351458516201747

21921393000146

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 28, 2017

24/02/2035

09/18/2025 19:00:01

REATIVO SECO VITROS* PARA TEOFILINA THEO
Risk Class III

Registration Details

81246986783

25351458516201747

21921393000146

Dates and Status

Aug 28, 2017

24/02/2035

09/18/2025 19:00:01

Companies Making Similar Products
Top companies providing products with the same technical name: "THEOPHYLLINE"