9 results
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20ms
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Sources: EU EUDAMED, US FDA
REPICCI LOCKED KEEL TIBIAL BEARING
FDA 510(k)
FDA Class 2
·Orthopedic
BUSCH®, BNA®
FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120304461·Diamond, cylinder round, medium grit
IMPLANTABLE ELECTRODE LEAD, MODEL 030-446
FDA 510(k)
FDA Class 3
·Cardiovascular
SYMMETRY AORTIC CLIP SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFICATION TO STRAIGHT-IN BONE SCREW FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EPIX UNIVERSAL CLIP APPLIER
FDA Adverse Event
APPLIED MEDICAL·Product code FZP·March 26, 2013
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·March 9, 2011
HILL-ROM 100 LOW BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·April 16, 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