BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    EMPI SINGLE USE

    FDA 510(k)
    FDA Class 2 ·Neurology

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011822224300·Ortho-Cast M-Series, buccal tube, double rectan...

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011822224400·Ortho-Cast M-Series, buccal tube, double rectan...

    COOL BOND LIGHT CURED BRACKET ADHESIVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    SurgiLance® Safety Lancet

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

    HS HAND CONTROLLED CURVED SHEA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC (CINCINNATI)·Product code GEI·December 3, 2007

    PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 20, 2014

    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