8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
CMW CEMENT PRESSURISATION SYSTEM
FDA 510(k)
FDA Class 1
·Orthopedic
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756739382·THORACOSCOPY PACK
PATIENT EXAMINATION GLOVE (LATEX)
FDA 510(k)
FDA Class 1
·General Hospital
FTK FECAL TRANSPORT KIT
FDA 510(k)
FDA Class 1
·Microbiology
REALSEAL SE
FDA Adverse Event
Injury
·SYBRONENDO·Product code KIF·June 26, 2014
VENTED AUTOFEED CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 11, 2010
DIGITAL RADIOGRAPHY CXDI-55C
FDA Adverse Event
Malfunction
·CANON, INC·Product code MQB·December 31, 2012
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system
FDA Enforcement
Class I
·Terminated·CareFusion 303, Inc.·August 12, 2020