BEUDAMED
    15 results · 27ms · 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.

    DACOMED CORP. ESKA-HERRMAN VOICE PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981125417·4.0mm Fixed Angle Screw, Self Tapping, 18mm

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209126569·

    MEDIAL PILON PLATE

    FDA UDI
    Biomet Orthopedics, LLC·00887868058271·

    MEDIAL PILON PLATE

    FDA UDI
    Biomet Orthopedics, LLC·00887868058288·

    MEDIAL PILON PLATE

    FDA UDI
    Biomet Orthopedics, LLC·00887868058240·

    MEDIAL PILON PLATE

    FDA UDI
    Biomet Orthopedics, LLC·00887868058257·

    MEDIAL PILON PLATE

    FDA UDI
    Biomet Orthopedics, LLC·00887868058264·

    MEDIAL PILON PLATE

    FDA UDI
    Biomet Orthopedics, LLC·00887868058295·

    THERAPEUTIC LIMB MANIPULATOR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    XMA INTEGRATED TABLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 6, 2014

    STERLING BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·October 5, 2010

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 3, 2012

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015