BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    OKLand Patient Return Electrode Pad

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

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00198506083778·KELLY RETRACTOR BLADE 3" X 4 1/2", RIGID SHAFT.

    DASH Flex 12 Centrifuge, MarketLab

    FDA UDI
    DRUCKER DIAGNOSTICS·00810052860213·General purpose laboratory centrifuge for sampl...

    AIDA DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TELECTRODE WET GEL ECG ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARTIVA IMPLANT

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·November 13, 2020

    CARTIVA IMPLANT

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·November 9, 2020

    ONE TOUCH ULTRASMART METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·December 22, 2009

    AO/ASIF-QC F/COMPACT AIR DRIVE+POWER DRI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·October 17, 2014

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 21, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·February 9, 2017

    ALPHA I INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·April 11, 1997