BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    AD150, AUTOMATED HEMATOLOGY DILUTOR

    FDA 510(k)
    FDA Class 1 ·Hematology

    300 Series Facebow

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746150739·FACEBOW LOOP STYLE SHORT OUTER BOW 045 SIZE 3 97MM

    Megasystem C

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575383498·Stem Components,Push-through, for total femur r...

    VITA VM LC Flow

    FDA 510(k)
    FDA Class 2 ·Dental

    QUILL NONABSORBABLE POLYPROPYLENE BARBED SUTURE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    QUILL SRS

    FDA Adverse Event
    Malfunction ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 17, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 5, 2014

    SPINBRUSH PRO WHITENING POWERED TOOTHBRUSH

    FDA Adverse Event
    Malfunction ·CHURCH & DWIGHT CO., INC.·Product code JEQ·November 13, 2012

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 29, 2010

    BD DISC CEFTAZIDIME CAZ-30 JAPAN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code JTN·January 18, 2022