Photometer - ANVISA Registration 10303460368
Access comprehensive regulatory information for Photometer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10303460368 and manufactured by HUMAN GMBH. The registration is held by IN VITRO DIAGNOSTICA LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including SINNOWA MEDICAL SCIENCE & TECHNOLOGY CO., LTD., BIOPLUS PRODUTOS PARA LABORATÓRIOS LTDA, and 3 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
10303460368
25351223607201006
42837716000198
Company Information
Dates and Status
Jan 24, 2011
VIGENTE
09/18/2025 19:00:01
Fotometro
ANALISADOR SEMI-AUTOMÁTICO BTS-350
BIOSYSTEMS S.A.
10300390345
Dec 17, 2018
Fotometro
Analisador Bioquimico Semi Automático Sinnowa
SINNOWA MEDICAL SCIENCE & TECHNOLOGY CO., LTD.
81452980009
Mar 12, 2018
Fotometro
ANALISADOR SEMI-AUTOMÁTICO PARA BIOQUÍMICA
BIOPLUS PRODUTOS PARA LABORATÓRIOS LTDA
10423910006
Nov 24, 2014

