BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    QUEX ED; QUEX S

    FDA 510(k)
    FDA Class 2 ·Neurology

    DC-N2/DC-N2S DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO: NUCAMMA RX

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·September 27, 2023

    GASTRONOMY TUBE 18F

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, INC.·Product code KNT·September 12, 2014

    UNKNOWN DEPUY PINNACLE HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code LPH·August 18, 2011

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 18, 2013

    HAND PIECE FOR BATTERY POWERED DRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·May 20, 2025

    TRIDENT PSL WITH PUREFIX HA

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·May 13, 2014

    TRIDENT 10° X3 INSERT 28MM ID

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 13, 2014