BEUDAMED
    712 results · 37ms · Sources: EU EUDAMED, US FDA

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    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·April 13, 2018

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 13, 2018

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 13, 2018

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 13, 2018

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 13, 2018

    HU-FRIEDY 5-68 BARNHART CURETTE, RESINEIGHT

    FDA Adverse Event
    Other ·HU-FRIEDY MFG. CO., LLC·Product code EKE·September 30, 2011

    HU-FRIEDY #2 MOLT SINGLE END CURETTE

    FDA Adverse Event
    Other ·HU-FRIEDY MFG. CO.,INC.·Product code EKE·October 11, 2011

    CURETTE, OPERATIVE

    FDA Adverse Event
    Malfunction ·SYMMETRYSURGICAL, INC.·Product code EKE·August 11, 2017

    HU-FRIEDY SG17/1898

    FDA Adverse Event
    Other ·HU-FRIEDY MFG. CO., LLC·Product code EKE·October 8, 2013

    HU-FRIENDLY SAS13/1498

    FDA Adverse Event
    Other ·HU-FRIEDY MFG. CO., LLC·Product code EKE·October 8, 2013

    AUTOMATED PLASMA APHERESIS MACHINE (RETURN-CYCLE SYSTEM WITH PRESSURE MONITORING

    FDA Adverse Event
    Injury ·UNK·Product code GKT·December 1, 2025

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 13, 2018

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 13, 2018

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·April 13, 2018

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 13, 2018

    CHARITE DISC REPLACEMENT

    FDA Adverse Event
    Injury ·DEPUY SPINE·Product code MJO·August 14, 2007

    Curette, Operative

    FDA classification
    FDA Class 1 ·Curette, Operative

    EEE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    EKF Life Sciences

    FDA registration
    EKF Life Sciences·3 products·🇺🇸 United States

    EKF DIAGNOSTIC GMBH

    FDA registration
    EKF DIAGNOSTIC GMBH·4 products·🇩🇪 Germany