Introduction to the MAUDE database.
Clin Obstet Gynecol
; 51(1): 120-3, 2008 Mar.
Article
em En
| MEDLINE
| ID: mdl-18303506
ABSTRACT
The Manufacturer and User Facility Device Experience (MAUDE) database represents a reporting system mandated by the Food and Drug Administration for postmarket surveillance. MAUDE has been made into a searchable online database that includes all reported events in which medical devices may have malfunctioned or caused a death or serious injury. For the clinician considering the use of a new medical device, searching the MAUDE database is useful to search for complications not yet reported in the medical literature.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Procedimentos Cirúrgicos em Ginecologia
/
Bases de Dados como Assunto
Limite:
Female
/
Humans
País/Região como assunto:
America do norte
Idioma:
En
Revista:
Clin Obstet Gynecol
Ano de publicação:
2008
Tipo de documento:
Article
País de afiliação:
Estados Unidos