7 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE
FDA 510(k)
FDA Class 2
·Orthopedic
M-XX OXYGEN SENSORS
FDA 510(k)
FDA Class 2
·Anesthesiology
EAR MUFFINS
FDA 510(k)
FDA Class 2
·Neurology
TAPERED SPACER ARTICUL/EZE -3
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LZY·April 23, 2013
CONSTELLATION WITH LASER
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CTR·Product code HQC·April 8, 2011
GEM III AT
FDA Adverse Event
Injury
·MEDTRONIC S.A.·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