BEUDAMED
    39 results · 31ms · Sources: EU EUDAMED, US FDA

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    MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198918·AK3 Congruent Insert Trial Size 1, 13mm

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482053096·Symmetry® Probe, w/Eye, Stainless Steel, 5 1/8 ...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450210642·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450226209·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450169094·

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310K0191130·Dilator, Large

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962108802·PROBE W/EYE, 5 1/8", SS

    HYDRAGEL ISO-PAL K20 (PN 3022); HYDRAGEL 7 ISO-PAL (PN 4112); HYDRAGEL 15 ISO-PAL (PN 4132)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    IVC THREE BLASTOCYST MEDIUM, CAT # 2007

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 4, 2013

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·December 23, 2014

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·November 22, 2014

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code OVD·April 21, 2018

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·May 10, 2013

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SWINNEA DC·Product code MAX·February 18, 2011

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code OVD·August 9, 2017

    PASSPORT 2 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code DSI·April 30, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 16, 2014

    M3155 RELEASE L.0 UPGRADE

    FDA Adverse Event
    Death ·PHILIPS HEALTHCARE·Product code MHX·May 6, 2011