BEUDAMED
    645 results · 27ms · Sources: EU EUDAMED, US FDA

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    Freedom(R) - TiNbN Coated Knee

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B5231003576200912·Lordotic TPLIF Cage, Titanium 20AP X 09ML X 12H...

    METZENBAUM SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896098183·METZENBAUM SCISSORS WITH GOLD SCREW FINE CURVED...

    Zavation

    FDA UDI
    Zavation LLC·00842166132009·Ti3Z CIF 12mmx14mmx12mm -9 deg

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021445·A-CIFT SoloFuse 4.5 Screw, Lag, 12mm

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100149200912·Non-Lordotic TPLIF Cage, Titanium 20AP X 09ML X...

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100035200912·PLIF CAGE, NON-LORDOTIC, 20AP X 09ML X 12HT

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100097200912·PLIF CAGE, LORDOTIC, 20AP X 09ML X 12HT

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B523100198200912·Lordotic Bullet Nose Cage, 20AP X 09ML X 12HT

    DISPOSABLE NERVE STIMULATING PROBE, BIPOLAR CONCENTRIC, DISPOSABLE NERVE STIMULATOR PROBE, BIPOLAR SIDE BY SIDE

    FDA 510(k)
    FDA Class 2 ·Neurology

    SIMPLICITY EASY SOFT INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B52310035712200912·Lordotic TPLIF Cage, Titanium 20AP X 09ML X 12H...

    PLIF Cage

    FDA UDI
    Eisertech, LLC·B52310035718200912·Lordotic TPLIF Cage, Titanium 20AP X 09ML X 12H...

    HEMOSPRAY ENDOSCOPIC HEMOSTAT

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code QAU·August 16, 2022

    HEMOSPRAY ENDOSCOPIC HEMOSTAT

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code QAU·March 14, 2022

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS·Product code MKJ·September 16, 2014

    GEM PREMIER 4000

    FDA Adverse Event
    Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code MZV·June 30, 2011

    PFC*SIGMA C/S NPOR FEM LT SZ 3

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 2, 2013

    AZURION

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 3, 2026

    AZURION

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·January 12, 2026