BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    RAY SACRAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377069016·RELINE C Screw, 4.5x20mm MA

    NP UCLA Abutment Waxing Sleeve, Non-Hexed

    FDA UDI
    STERNGOLD DENTAL LLC·00841549111808·The UCLA-Type Abutment is attached directly to ...

    SCHWERT

    FDA UDI
    A. Schweickhardt GmbH & Co. KG·E89619045200·Bowmann lachrymal probe, Silver, cylind...

    Solstice Occipito-Cervico-Thoracic System

    FDA UDI
    Life Spine, Inc.·00190837014728·

    Rampart One Lumbar Interbody Fusion Device

    FDA UDI
    SPINEOLOGY INC.·M7404904520·Rampart One Screw

    MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    WURTZ CHOLEY CLIP (TM)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    OXF ANAT BRG RT MD SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 9, 2019

    OXF UNI TIB TRAY SZ D RM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 9, 2019

    OXF TWIN-PEG CMNTD FEM MD PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 9, 2019

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 22, 2010

    INCEPTA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014

    GOBED+

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·November 30, 2012

    TPRLC 133 FP TYPE1 PPS HO 17.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·April 6, 2023