AMMONIA - ANVISA Registration 81246980004
Access comprehensive regulatory information for AMMONIA in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81246980004 and manufactured by ORTHO CLINICAL DIAGNOSTIC, 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 ROCHE DIAGNOSTICS 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.
Device Details
Registration Details
81246980004
25351455192201795
21921393000146
Company Information
Dates and Status
Aug 28, 2017
VIGENTE
09/18/2025 19:00:01
AMÔNIA
Família Amônia
KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO LTDA
10377390268
Jan 27, 2025
AMÔNIA
Família Amônia Plus
BIOTECNICA INDUSTRIA E COMERCIO LTDA
80027310341
Sep 16, 2024
AMÔNIA
AMMONIA TEST KIT II
ARKRAY FACTORY INC
80430080019
Jul 10, 2023
AMÔNIA
Família Amônia - AMN
BIOTECNICA INDUSTRIA E COMERCIO LTDA
80027310303
Apr 22, 2021
AMÔNIA
NH3L2
ROCHE DIAGNOSTICS GMBH
10287411515
Jul 13, 2020

