BEUDAMED
    7,970 results · 31ms · Sources: EU EUDAMED, US FDA

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    Quest Diagnostics Oral Fluid Oxycodone HEIA

    FDA UDI
    Quest Diagnostics·00868586000292·

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902133226·Pressure Injectable Three-Lumen CVC Kit

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902207590·FlexTip Plus(R) Epidural Catheterization Kit

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902114300·FlexTip Plus(R) Epidural Catheterization Kit

    LIFECARE PCA

    FDA Adverse Event
    ABBOTT LABORATORIES·Product code MEA·December 21, 1993

    ENSEAL X1 TISSUE SEALER

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GEI·November 7, 2022

    ENSEAL X1 TISSUE SEALER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·November 7, 2022

    PVH C-SECTION PACK

    FDA Adverse Event
    Malfunction ·MAXXIM MEDICAL·Product code LRO·October 31, 2001

    BD INSYTE-N AUTOGUARD WINGED

    FDA Adverse Event
    BD·Product code FOZ·November 4, 2022

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code IOR·May 24, 2013

    VISUALASE

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC.·Product code GEX·June 26, 2025

    BD INSYTE AUTOGUARD-N WINGED CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 5, 2022

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·TAIWAN AN I CO.,LTD.·Product code IOR·September 30, 2013

    Pressure Injectable Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-15703-PVH and ASK-15703-PNYP

    FDA Enforcement
    Class II ·Terminated·Arrow International Inc·June 6, 2018

    IN.PACT ADMIRAL PACLITAXEL-ELUTING PTA BALLOON CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code ONU·March 11, 2025

    UNKNOWN PROTACK

    FDA Adverse Event
    Injury ·US SURGICAL PUERTO RICO·Product code GDW·June 26, 2019

    UNKNOWN ABSORBATACK

    FDA Adverse Event
    Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·June 26, 2019

    SUMMIT POR TAPER SZ8 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 31, 2020

    UNK HIP FEMORAL STEM SROM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 23, 2021

    SIG RP AOX STB INS SZ2.5 17.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·July 20, 2020