BEUDAMED
    15 results · 19ms · 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.

    SARNS 9000 HEART-LUNG CONSOLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556706128·GC Initial™ LF Shoulder Transpa ST-31, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228711311·GC Initial™ LF Shoulder Transpa ST-31, 20g

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771012450·K-Wires, Single trocar, .035-inch (.9mm) diamet...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292688·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049033·K-Wires, Single trocar, .035-inch (.9mm) diamet...

    K-Wire w. trocar/round end 0.89mm/102mm, 6 pcs./unit

    FDA UDI
    mahe medical gmbh·EMAHKM711310·K-Wire w. trocar/round end 0.89mm...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659484221·K-Wire w. trocar/round end _x000D_...

    ORTHOSOURCE

    FDA UDI
    ORTHOSOURCE·D9118711310·Superb Tweed Arch

    UNO

    FDA 510(k)
    FDA Class 2 ·Dental

    MHC Standard and NRFit Tip Syringes

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROG VALVE CLYNDRICAL

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·April 5, 2023

    ENDURON 10D 60 OR 72ODX28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.-1818910·Product code LPH·June 13, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 12, 2012

    VITALITY

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 15, 2010