BEUDAMED
    9 results · 22ms · 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 ×

    STAT DL 10.5 FR. 50 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·August 27, 1998

    ECLIPSE TRUNION 43MM, SLOTTED, TPS CAP

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code QHQ·February 8, 2024

    ECLIPSE SHOULDER PROSTHESIS

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code QHQ·February 8, 2024

    UNIVERS VAULTLOCK GLENOID, SMALL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code KWS·January 3, 2024

    ARTHREX ECLIPSE HUMERAL HEAD, 43/16

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code QHQ·January 3, 2024

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 8, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·October 17, 2012

    HARMONIC ACE 23CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 16, 2010

    EQUINOXE REVERSE 38MM GLENOSPHERE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·December 18, 2023