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

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    MICROTEK PROBE DRAPE

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

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867386587·Cortical Screw, 2.7 mm x 24 mm

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867046801·LO-PRO SCRW TM SS 2.7X 24MMCORTEX

    CelerityTM 10 STEAM Chemical Indicator

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEWPORT HTS50 VENTILATOR WITH DUAL PAC BATTERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXTRUS 4137

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO, KG·Product code NVZ·October 22, 2010

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·December 20, 2012

    SYMBIQ SINGLE CHANNE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD·Product code FRN·April 10, 2014

    TFNA HELICAL BLADE 105MM STERILE

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HSB·February 17, 2017

    LO-PRO LOCK SCRW,SS 2.7X 16MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 4, 2026

    LO-PRO LOCK SCRW,SS 3.5X 14MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 4, 2026

    LO-PRO LOCK SCRW,SS 2.7X 14MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 4, 2026

    LO-PRO LOCK SCRW,SS 2.7X 18MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 4, 2026

    LO-PRO LOCK SCRW,SS 3.5X 18MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 4, 2026