BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    BREATHING FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MONDEAL

    FDA UDI
    MONDEAL Medical Systems GmbH·04050435062438·MCD Screw 3.0 x 18 mm M2 non lo...

    SFI-ANCHOR

    FDA 510(k)
    FDA Class 2 ·Dental

    WILSON-COOK CELIAC PLEXUS NEUROLYSIS NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ECHOTIP CELIAC PLEXUS NEUROLYSIS NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code BSP·November 21, 2019

    RESTORE SENSOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 23, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 13, 2012

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

    CRTS SM IL SG VLV ONLY

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·June 23, 2021

    ECHOTIP ULTRA CELIAC PLEXUS NEUROLYSIS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·July 5, 2023

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018