CANNABINOID - ANVISA Registration 81246980018
Access comprehensive regulatory information for CANNABINOID in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81246980018 and manufactured by ORTHO CLINICAL DIAGNOSTICS, INC.. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ASSURE TECH. HANGZHOU CO., LTD., GUANGZHOU WONDFO BIOTECH CO., LTD., 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.
Device Details
Registration Details
81246980018
25351455301201774
21921393000146
Company Information
Dates and Status
Aug 28, 2017
VIGENTE
09/18/2025 19:00:01
CANABINÓIDE
Dia Sure K2
ASSURE TECH. (HANGZHOU) CO., LTD
80277090062
Jul 10, 2023
CANABINÓIDE
THC RAPID TEST
HANGZHOU ALLTEST BIOTECH CO., LTD
80638720206
Dec 09, 2021
CANABINÓIDE
Rapid THC Test
XIAMEN BOSON BIOTECH CO., LTD
82036180014
Jan 14, 2021
CANABINÓIDE
CANNABI-Screen®
VEDALAB
80464810749
Dec 17, 2020
CANABINÓIDE
Família Alinity c Cannabinoids
MICROGENICS CORPORATION
80146502280
Aug 31, 2020

