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

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    Hemo Control (optional Add Pack Hemo Control DM)

    FDA 510(k)
    FDA Class 2 ·Hematology

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B5231003576200909·Lordotic TPLIF Cage, Titanium 20AP X 09ML X 09H...

    Zavation

    FDA UDI
    Zavation LLC·00842166131972·Ti3Z CIF 12mmx14mmx9mm -9 deg

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100035200909·PLIF CAGE, NON-LORDOTIC, 20AP X 09ML X 09HT

    Cortina

    FDA UDI
    NEUROSTRUCTURES, INC·00841508104438·PLIF Cage, Non-Lordotic 20mm x9mm x09mm

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100149200909·Non-Lordotic TPLIF Cage, Titanium 20AP X 09ML X...

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100097200909·PLIF CAGE, LORDOTIC, 20AP X 09ML X 09HT

    ZAVATION

    FDA UDI
    Zavation LLC·00842166104068·CIF 12x14, 9 deg, -09

    Cortina

    FDA UDI
    NEUROSTRUCTURES, INC·00841508104759·BN PLIF Cage, 4 Deg-Lordotic 20mmx9mmx9mm

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100198200909·Lordotic Bullet Nose Cage, 20AP X 09ML X 09HT

    Squadron Lumbar Cage

    FDA UDI
    VALORUS SPINE LLC·00811771036941·Squadron Lordotic Bullet Nose PLIF Cage, 20mm x...

    Squadron Lumbar Cage

    FDA UDI
    VALORUS SPINE LLC·00811771035142·Squadron Parallel Bullet Nose PLIF Cage, 20mm x...

    Squadron Lumbar Cage

    FDA UDI
    VALORUS SPINE LLC·00810065990020·Squadron Anatomical Bullet Nose PLIF Cage, 20mm...

    REPROCESSED COMPRESSION SLEEVES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HDM99

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ARCHITECT CA 19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code NIG·November 7, 2016

    FLAIR ENDOVASCULAR STENT GRAFT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code MIH·September 12, 2014

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·June 30, 2011

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

    NEEDLE 30X1 RB

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·October 14, 2021