BEUDAMED
    22 results · 22ms · Sources: EU EUDAMED, US FDA

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    COOK VASCULAR INC. VITAL-PORT VASCULAR ACCESS SYSTEM POWER INJECTABLE PORT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·November 4, 2015

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·November 17, 2017

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LIT·May 23, 2016

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517284259·CoRoent® LO Ti, 14x10x25mm 5°

    X-Box

    FDA UDI
    INNO Holdings, Inc.·M71190814250·PEEK, Ta

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X0814250·8mm H x 14mm W x 25mm L x 0 degrees XLIF

    n/a

    FDA UDI
    Ortho Development Corporation·00822409075539·12/14 Press-Fit Broach 14x25

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L081425120·8mm H x 14mm W x 25mm L XLIF Trial 12 degree Lo...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X08142580·8mm H x 14mm W x 25mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X081425120·8mm H x 14mm W x 25mm L x 12 degrees XLIF

    GENTLEWAVES LED PHOTOMODULATION DEVICE

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

    CARMEN

    FDA 510(k)
    FDA Class 2 ·Dental

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·April 26, 2013

    AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Injury ·INVAMEX·Product code FNG·April 29, 2011

    MEDTRONIC FIDELIS DEFIB LEAD

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code LWS·July 25, 2008

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 11, 2019