AMPHETAMINE - ANVISA Registration 80277090012

Access comprehensive regulatory information for AMPHETAMINE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80277090012 and manufactured by AMERICAN BIO MEDICA CORPORATION. The registration is held by GRIMEXTUR- IMPORTAÇÃO E EXPORTAÇÃO DO BRASIL LTDA ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SIEMENS HEALTHCARE DIAGNOSTICS INC., 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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80277090012
Registration Details
ANVISA Registration Number: 80277090012
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

RAPID DRUG SCREEN - RDS® - AMP-COC-OPI300-METH-THC
Risk Class II

Registration Details

80277090012

25351620836201427

07236937000100

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 22, 2014

VIGENTE

09/18/2025 19:00:01