10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
TITANIUM MESH
FDA 510(k)
FDA Class 2
·Neurology
Brigade
FDA UDI
Nuvasive, Inc.·00887517962973·Brigade Lateral Trial, 10x34x32mm 30°
CARE PROVIDER STATION ADDITION OF WEIGHT SCALE
FDA 510(k)
FDA Class 2
·Cardiovascular
VESISCAN
FDA 510(k)
FDA Class 2
·Radiology
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·April 8, 2025
SWIFTSET TOPICAL SKIN ADHESIVE
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code MPN·July 9, 2015
VASO VIEW HEMOPRO
FDA Adverse Event
Injury
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·January 3, 2013
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 26, 2007
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·April 14, 2015
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