METHOTREXATE - ANVISA Registration 80146501923

Access comprehensive regulatory information for METHOTREXATE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80146501923 and manufactured by ABBOTT GMBH. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until Mar 16, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 3 companies making the same product including ABBOTT GMBH, SIEMENS HEALTHCARE 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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80146501923
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Registration Details
ANVISA Registration Number: 80146501923
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

ARCHITECT Methotrexate Reagent Kit
Risk Class III

Registration Details

80146501923

25351773225201463

56998701000116

Company Information

ABBOTT GMBH
Germany
PT: ALEMANHA

Dates and Status

Mar 16, 2015

16/03/2035

09/18/2025 19:00:01

ARCHITECT Methotrexate Reagent Kit
Risk Class III

Registration Details

80146501923

25351773225201463

56998701000116

Company Information

Dates and Status

Mar 16, 2015

16/03/2035

09/18/2025 19:00:01