BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    METER C - OT PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·December 6, 2001

    IMPL TAPERED SCR-V SBM 3.7MM 3.5MM 10MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·October 13, 2022

    MPL TAPERED SCR-V SBM 3.7MM 3.5MM 10MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·July 11, 2023

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code OYC·June 24, 2019

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·May 14, 2015

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 6, 2014

    SPECTRANETICS LEAD LOCKING DEVICE

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code DRB·July 26, 2013

    UNKNOWN ZIMMER NAIL

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code HAO·November 25, 2015