PHENYTOIN - ANVISA Registration 80254180459

Access comprehensive regulatory information for PHENYTOIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180459 and manufactured by manufacturer not specified. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Jul 03, 2033.

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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80254180459
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Registration Details
ANVISA Registration Number: 80254180459
Janaina dos Santos de Miranda

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Related Devices (2)

CEDIA Phenytoin II Assay
Risk Class III

Registration Details

80254180459

25351151977202330

04930429000139

Company Information

Dates and Status

Jul 03, 2023

03/07/2033

09/18/2025 19:00:01

CEDIA Phenytoin II Assay
Risk Class III

Registration Details

80254180459

25351151977202330

04930429000139

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 03, 2023

03/07/2033

09/18/2025 19:00:01

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