BEUDAMED
    14 results · 25ms · Sources: EU EUDAMED, US FDA

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    SCIMED R30 SILICONE ASSIST RESERVOIR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867386563·Cortical Screw, 2.7 mm x 20 mm

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867046788·LO-PRO SCRW TM SS 2.7X 20MMCORTEX

    TRACHEAL INTUBATION FIBERVIDEOSCOPE, MODELS LF-Y0004 AND LF-Y0005

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Freedom Spinal Cord Stimulator (SCS) System

    FDA 510(k)
    FDA Class 2 ·Neurology

    GEMSTR 7 THPY ALT ST

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

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·October 21, 2010

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 20, 2012

    LO-PRO SCRW TM SS 2.7X 20MMCORTEX

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

    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