BEUDAMED
    92 results · 23ms · Sources: EU EUDAMED, US FDA

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    O-arm O2 Imaging System

    FDA 510(k)
    FDA Class 2 ·Radiology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694005999·2.4mm Screw VISIDISK (GREEN)

    DEBAKEY NEEDLE PULLING TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896084476·DEBAKEY NEEDLE PULLING TISSUE FORCEPS WITH TUNG...

    Greenwald Surgical Company, Inc.

    FDA UDI
    GRACE MANUFACTURING, INC.·10801334013325·STORZ S/S SPIKED ROLLER ELECTRODE Model # ...

    KAYE FACE LIFT/BLEPHAROPLASTY SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896054394·KAYE FACE LIFT/BLEPHAROPLASTY SCISSORS CURVED B...

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, PLASMA SCALPEL GS, TURBOVAC GS

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

    Widex

    FDA UDI
    Widex A/S·05706069689440·Widex BEYOND B-F2 (Midnight black ) Telecoil, R...

    CRYOMACS FREEZING BAG 250

    FDA Adverse Event
    Malfunction ·MILTENYI BIOTEC B.V. & CO. KG·Product code KSR·March 2, 2021

    BD VACUTAINER® URINE ANALYSIS PRESERVATIVE TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JTW·July 20, 2023

    BIPOLAR DISSECTION ELECTRODE

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code GCJ·June 14, 2023

    COAGULATING AND DISSECTING ELECTRODE

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code KNF·June 13, 2023

    INSERT

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code GCJ·June 23, 2023

    FIBER OPTIC LIGHT CABLE

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code FCW·July 10, 2023

    COAGULATING AND DISSECTING ELECTRODE

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code KNF·June 13, 2023

    ULTRAMICRO NEEDLE HOLDER, SIZE 3 MM

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code GCJ·June 19, 2023

    SUPRALOOP REPLACEMENT SLING

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code KNF·June 14, 2023

    STANDARD-OBTURATOR

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code HET·June 27, 2023

    COAGULATION & DISSECTION ELECTRODE

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code KNF·June 14, 2023

    STONE CRUSHING FORCEPS, SGL. ACTION JAWS

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code OCZ·June 7, 2023