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

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    Miromatrix Biological Mesh TW

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

    RC Basal Screw , for Cem.abutment only

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600307761·

    BOWMAN LACRIMAL PROBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896018600·BOWMAN LACRIMAL PROBE SIZE 5-6 BUTTERFLY HANDLE...

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PATIENT CONTOURED MESH (PCM)

    FDA 510(k)
    FDA Class 2 ·Neurology

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·October 7, 2014

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 14, 2011

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON INC·Product code OTN·June 11, 2013

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·December 5, 2025

    KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

    FDA 510(k)
    FDA Class 2 ·Neurology