BEUDAMED
    27 results · 22ms · Sources: EU EUDAMED, US FDA

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    pjur WOMAN Aloe, pjur analyse me! water-based, pjur BACK DOOR water-based, pjur med Moisturising glide,pjur med NATURAL glide, We-Vibe Lube made by pjur

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Trial Tibial Augment

    FDA UDI
    ADLER ORTHO SPA·08056269043625·TRIAL PANTHEON TIBIAL AUGMENT RM/LL SIZE 7 H5

    BAILEY HEMOSTATIC FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896084858·BAILEY HEMOSTATIC FORCEPS ACUTE ANGLED EXTRA FI...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153160281·TENSION SHEATH

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694006859·Holding Cap, Serrated, Blunt Cannula

    ACCUCLOT DRVVT SCREEN, CATALOG NO. A6094

    FDA 510(k)
    FDA Class 1 ·Hematology

    HORIZON PHACOEMULSIFICATION SYSTEM, MODEL HZN-2030

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AUVON TENS & EMS DEVICE

    FDA Adverse Event
    Injury ·SHEN ZHEN AS TEC TECHNOLOGY CO LTD·Product code NUH·January 28, 2025

    21 G X 1.25 IN BD ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·November 27, 2017

    PROSTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code KNS·October 30, 2009

    PROSTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code KNS·October 30, 2009

    PROSTIVA

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code KNS·October 30, 2009

    PROSTIVA

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code KNS·October 30, 2009

    PROSTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code KNS·October 30, 2009

    PROSTIVA

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code KNS·October 30, 2009

    21 G X 1.25 IN BD ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH LUER ADAPTER

    FDA Adverse Event
    Injury ·BECTON, DICKINSON & CO., (BD)·Product code FMI·March 1, 2016

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    CELSIUS THERMOCOOL

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·August 11, 2011

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·July 1, 2013

    VALVE CONTEGRA

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·May 23, 2017