BEUDAMED
    14 results · 28ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    NUTRIENT BROTH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    TSRH® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978042756·CROSSLINK 811-323 LP MLTSP PL L 2.152.95

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962102114·ETHOS INTERFERENCE SCREW, PEEK, 13.0mm x 23mm

    SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS

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

    HIGH SENSITIVITY CORTISOL ENZYME IMMUNOASSAY, MODEL 1-0101/1-0102

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·April 8, 2011

    MSD - UNKNOWN IMPLANT

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·February 27, 2007

    ATTAIN ABILITY

    FDA Adverse Event
    Death ·MPRI·Product code OJX·May 15, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 15, 2007

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·October 31, 2012

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 18, 2023

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 7, 2023

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·November 14, 2023

    CD HORIZON

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA·Product code KWP·November 19, 2014