BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    WECK LX TM SKIN STAPLER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209115983·

    Arm automatic blood pressure monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code KNS·May 10, 2022

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·March 26, 2014

    PROXIMATE** RELOADABLE LINEAR CUTTER WITH SAFETY LOCK-OUT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 4, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 29, 2012

    ACUSNARE POLYPECTOMY SNARE SOFT

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code KNS·July 13, 2023

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code KNS·May 4, 2022