AMPHETAMINE - ANVISA Registration 82036180015
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 82036180015 and manufactured by XIAMEN BOSON BIOTECH CO., LTD. The registration is held by CONNECT ASSUNTOS REGULATÓRIOS, COMÉRCIO E DISTRIBUIDORA DE PRODUTOS MÉDICO-HOSPITALRES LTDA 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 AMERICAN BIO MEDICA CORPORATION, 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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🇧🇷 Brazil Regulatory Expert
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Registration Details
82036180015
25351821668202177
37026700000165
Company Information
Dates and Status
Jan 14, 2021
VIGENTE
09/18/2025 19:00:01
AMPHETAMINE
ANFETAMINA RAPID TEST
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AMPHETAMINE
RAPID TOX® - AMPHETAMINES (AMP)
AMERICAN BIO MEDICA CORPORATION
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SYVA RAPIDTEST D.A.U ANFETAMINAS (AMP)
SIEMENS HEALTHCARE DIAGNIOSTICS INC.
10345161209
Aug 10, 2009
AMERICAN BIO MEDICA CORPORATION• United States of America
SIEMENS HEALTHCARE DIAGNOSTICS INC.• United States of America
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ABON BIOPHARM CO. LTD• China
LABORLAB PRODUTOS PARA LABORATÓRIOS LTDA EPP• Brazil
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DOA AMP ECO Teste
Eco Diagnostica Ltda
80954880115
Jun 10, 2019
ANFETAMINA
ANFETAMINA RAPID TEST
GUANGZHOU WONDFO BIOTECH CO., LTD
80638720110
Jun 03, 2019