BEUDAMED
    10 results · 18ms · 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 Regulation: Us FDA ×

    MS EMULSION

    FDA 510(k)
    FDA Class 2 ·Dental

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123090·K-WIRE - DOUBLE TROCAR 1.2mm DIA x 75mm

    SYNTHES PANGEA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    WHOLEY HI-TORQUE GUIDE WIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDO CATCH GOLD

    FDA Adverse Event
    Injury ·DAVIS & GECK CARIBE LTD·Product code GCI·June 11, 2018

    TI PANGEA LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·June 5, 2012

    VIRTUOSO VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 9, 2013

    TRIMA ACCEL AUTOMATED BLOOD COLLECTION SET

    FDA Adverse Event
    Other ·CARIDIANBCT·Product code GKT·December 29, 2010

    ELITE & USA COLD KNIFE STRAIGHT BLADE

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code FJL·November 26, 2013

    TI PANGEA LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·June 5, 2012