BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    CUSTOMED LAP PACK I

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Synergy

    FDA UDI
    Rmo, Inc.·00885797375872·COLUMBIA SYN ROTH 022 HK2345

    HOTWIRE™ RF GUIDEWIRE

    FDA UDI
    Atraverse Medical, Inc·00850057445541·The HOTWIRE™ is a sterile, single-use guidewire...

    Rampart One Lumbar Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7404902029·Rampart One Trial, 14mm, M, 16°

    ZOLL M SERIES NIBP OPTION, MODEL MSERIES NIBP OPTION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENTSTAR RESUSCITAIRE, MODEL MP00311, VENTSTAR RESUSCITAIRE CEU, MODEL MP00310

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 4, 2024

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014

    ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 19, 2016

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 1, 2016

    XLD 110V L.A. NEW

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 7, 2014

    BIORAPTOR KNOTLESS

    FDA Adverse Event
    Malfunction ·MANSFIELD MANUFACTURING SITE·Product code MBI·January 8, 2013

    MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·November 12, 2010