BEUDAMED
    9 results · 28ms · 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.

    LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EBV-VCA-IGM IFA TEST SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DMS 300-2W HOLTER ECG RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PINN CAN BONE SCREW 6.5MMX15MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    SUMMIT POR TAPER SZ6 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    PINN CAN BONE SCREW 6.5MMX25MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·January 29, 2013

    LINOX SD 65/16

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO KG·Product code LWS·December 13, 2010

    UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 14, 2014