BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    CAUTERY; LOW TEMPERATURE (FINEADJUSTABLE FINE TIP, ELONGATED FINE TIP, MICRO FINE TIP)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AF541

    FDA UDI
    Respironics, Inc.·00606959024700·AF541 Under Nose Cushion, SIZE C, RP

    MaxFuse VBR, 10 (D) x 12 (W) x 53 (H)

    FDA UDI
    Pioneer Surgical Technology, Inc.·00846468055615·10 (D) x 12 (W) x 53 (H)

    UNIMAX VERESS NEEDLE

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

    RADIUS SNARE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929038864·Corpectomy, 12Dx14Wx41H 6°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929064757·Corpectomy, 12Dx14Wx41H 0°

    JOSTENT GRAFTMASTER

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·August 13, 2010

    PERCLOSE PROSTYLE SUTURE-MEDIATED CLOSURE AND REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·May 2, 2023

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·August 22, 2022

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 29, 2014

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 6, 2011

    PERCLOSE PROSTYLE SUTURE-MEDIATED CLOSURE AND REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·May 2, 2023