8 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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ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32
FDA 510(k)
FDA Class 2
·Orthopedic
SOLOBOND PLUS
FDA 510(k)
FDA Class 2
·Dental
ARTHRO-SURGIMAT-A103
FDA 510(k)
FDA Class 2
·Orthopedic
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 18, 2024
UNKNOWN OUTBACK
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code DQY·April 2, 2013
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·July 31, 2014
ZMR HIP SYSTEM FEMORAL STEM REVISION TAPER
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWY·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