FDA updates fields available in the Manufacturer and User Facility Device Experience (MAUDE) database and openFDA

Press releases may be edited for formatting or style | November 07, 2022 Health IT Risk Management

The U.S. Food and Drug Administration (FDA) updated its public adverse event databases to include fields for the Unique Device Identifier – Device Identifier (UDI-DI) and a modified version of the complete Unique Device Identifier (UDI-Public) in the search results.

The new fields are now available in the Manufacturer and User Facility Device Experience (MAUDE) database and the openFDA Device Adverse Event endpoint. This latest update is intended to ensure adverse event information in the databases is searchable.

We repair MRI Coils, RF amplifiers, Gradient Amplifiers and Injectors.

MIT labs, experts in Multi-Vendor component level repair of: MRI Coils, RF amplifiers, Gradient Amplifiers Contrast Media Injectors. System repairs, sub-assembly repairs, component level repairs, refurbish/calibrate. info@mitlabsusa.com/+1 (305) 470-8013



You Must Be Logged In To Post A Comment Entrar Se você já criou uma conta, use seu endereço de e-mail e senha para entrar usando o formulário abaixo. Problemas de login: Estale aqui se você estiver tendo problemas de login. Endereço de email: Senha: Esqueceu sua senha? Problemas de login? Veja nosso Notícia legal e Aviso de privacidade Registo O registro é gratuito e fácil. Aproveite os benefícios dos principais produtos novos e inovadores do mundo. Mercado de equipamentos médicos usados. Registrar agora!