BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    SOOTHIES GEL PADS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    XIA SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    XIA SCREW 6, 5 X 40

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code MNI·May 11, 2011

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·September 17, 2013

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 2, 2013

    SCD EXPRESS SLEEVE T/L MEDIUM

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE / KENDALL·Product code JOW·May 27, 2008

    UNKNOWN DEPUY CEMENT

    FDA Adverse Event
    Injury ·DEPUY CMW·Product code LOD·April 7, 2011

    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