9 results
·
27ms
·
Sources: EU EUDAMED, US FDA
OPDIMA DIGITAL MAMMOGRAPHIC X-RAY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
VENTRIX TRUE TECH VENTRICULAR TUNNELING PRESSURE MONITORING KIT, MODEL NL960-V
FDA 510(k)
FDA Class 2
·Neurology
DISPOSABLE SURGICAL EXTENSION CABLE, MODEL 4255 AND MODEL 4260
FDA 510(k)
FDA Class 2
·Cardiovascular
ETEST DAPTOMYCIN DPC 256 WW S30
FDA Adverse Event
Malfunction
·BIOMÉRIEUX SA·Product code JWY·October 30, 2020
ETEST DAPTOMYCIN DPC 256 WW S30
FDA Adverse Event
Malfunction
·BIOMÉRIEUX SA·Product code JWY·October 30, 2020
BD INSYTE
FDA Adverse Event
Injury
·BD·Product code FOZ·April 19, 2013
PULSE GEN MODEL 102
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·April 8, 2011
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·July 10, 2008
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012