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

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    LOGIQ E9, LOGIQ E9 XDClear 2.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    2.0 LACTOSORB SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036055127·

    K162309

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code PGW·November 14, 2019

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295057697·ATTUNE KNEE SYSTEM REVISION TIBIAL AUGMENT UNIV...

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295057703·ATTUNE KNEE SYSTEM REVISION TIBIAL AUGMENT 10MM...

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295057734·ATTUNE KNEE SYSTEM REVISION TIBIAL AUGMENT 15MM...

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295057727·ATTUNE KNEE SYSTEM REVISION TIBIAL AUGMENT 10MM...

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295057710·ATTUNE KNEE SYSTEM REVISION TIBIAL AUGMENT 15MM...

    DIGITAL RADIOGRAPHY

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 26, 2024

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 15, 2024

    THERAKOS XTS PHOTOPHERESIS SYSTEM

    FDA Adverse Event
    Malfunction ·THERAKOS, INC.·Product code LNR·October 3, 2014

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 7, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·June 23, 2011

    ARCOM 28MM RNGLOC LNR HWALL 23

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 20, 2024

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·March 18, 2019

    UNKNOWN CUP

    FDA Adverse Event
    Injury ·.·Product code LPH·March 20, 2024

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 20, 2024

    UNKNOWN NGP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZP·April 10, 2025