BEUDAMED
    10 results · 34ms · Sources: EU EUDAMED, US FDA

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    LIFECOIL CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517963130·Brigade Lateral Trial, 9x38x28mm 10°

    CELLSEARCH CIRCULATING TUMOR CELL KIT MODEL 7900001

    FDA 510(k)
    FDA Class 2 ·Immunology

    VARI-LASE ENDOVENOUS LASER CONSOLE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CADD-SOLIS VIP AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FRN·March 24, 2026

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·December 4, 2020

    EGIA ULTRA UNIVERSAL STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·July 9, 2015

    SENSOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EZB·January 6, 2013

    CSS CANNULATED SCREW SYSTEM

    FDA Adverse Event
    Injury ·ORTHOHELIX SURGICAL DESIGN·Product code HWC·November 16, 2010

    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