9 results
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20ms
·
Sources: EU EUDAMED, US FDA
UCA CREAM PRODUCT REFORMULATION
FDA 510(k)
FDA Class 2
·Neurology
KETAC-CEM IN REF. TO K802048
FDA 510(k)
FDA Class 2
·Dental
ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACK
FDA 510(k)
FDA Class 2
·Cardiovascular
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
CONNECTION SCREW FOR PFNA AIMING ARM
FDA Adverse Event
Malfunction
·SYNTHES BETTLACH·Product code LXH·September 17, 2014
HUT EXT DR FINAL ASSY-RECERSE
FDA Adverse Event
Malfunction
·LIEBEL FLARSHEIM·Product code IXR·February 25, 2014
PRECISION XTRA/OPTIUM
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·September 18, 2007
PINNACLE
FDA Adverse Event
DEPUY, INC.·Product code KWA·September 17, 2012
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