8 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACE WIRE TENSION CLAMP
FDA 510(k)
FDA Class 2
·Orthopedic
IMMULITE 2000 3GALLERGY SPECIFIC IGE ASSAY KIT, MODEL L2KUN6
FDA 510(k)
FDA Class 2
·Immunology
PROGENY FORGED COCR CEMENTED FEMORAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
S-ICD SYSTEM
FDA Adverse Event
Malfunction
·CAMERON HEALTH INC·Product code NVY·May 7, 2014
UNKNOWN DEPUY BONE CEMENT
FDA Adverse Event
Injury
·DEPUY CMW ¿ REG. # 9610921·Product code LOD·January 8, 2013
MINI-CAP, DISCONNECT W/PVP-1SOLUTION
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·November 18, 2010
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·January 1, 2026
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