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

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    NERVE STIMULATOR MODEL AA 1050

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Cabo

    FDA UDI
    Seaspine Orthopedics Corporation·10889981160913·Variable -4.0mm Self Drilling, 14mm

    Cabo™

    FDA UDI
    NEUROSTRUCTURES, INC·00841508101864·Variable - 4.0mm Self Drilling 14mm

    A-FIT®

    FDA UDI
    Gc Orthodontics America Inc.·E53581161400001·A-FIT® 1. MOLAR UPR RGT SZ 14

    CABO ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·SEASPINE INC.·Product code KWQ·June 24, 2020

    CENTRICITY PERINATAL AND CENTRICITY INTENSIVE CARE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Sterling Supreme Diode Laser

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

    ZENIX

    FDA UDI
    Zoll Medical Corporation·00198843000384·ZENIX, HOSPITAL CRITICAL CARE TRANSPORT CONFIGU...

    ZENIX

    FDA UDI
    Zoll Medical Corporation·00812394022984·ZENIX, HOSPITAL CRITICAL CARE TRANSPORT CONFIGU...

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 15, 2014

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·October 31, 2012

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·August 23, 2010

    PSS Select medical products***Biopsy Punches*** Disposable manual instrument for skin biopsy.

    FDA Enforcement
    Class II ·Terminated·Clorox Healthcare Holdings, LLC (dba HealthLink)·July 10, 2013