BEUDAMED
    92 results · 23ms · Sources: EU EUDAMED, US FDA

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    POWDER FREE LATEX STERILE PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809845631·FOR MEN 20-30 MM HG KNEE HIGH OPEN TOE LARGE-LO...

    NA

    FDA UDI
    Stryker GmbH·00886385005782·Lag Screw, Non-Locking, Self-tap., T6 Drive

    INVOTEC INTERNATIONAL, INC.

    FDA registration
    INVOTEC INTERNATIONAL, INC.·34 products·🇺🇸 United States

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780486992·Integra® Miltex® Hank Uterine Dilator, 10-1/2",...

    E-SCAN MRI SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    AUDIOTRAVELLER, MODEL AA222

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 22, 2017

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 26, 2017

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·June 9, 2017

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·March 8, 2019

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 26, 2018

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·November 8, 2019

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 11, 2013

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTL. LTD.·Product code KWA·April 7, 2011

    RADIAL JAW 3 BIOPSY FORCEP W/NEEDLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNW·May 23, 2008

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·March 8, 2019

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 18, 2013

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·October 18, 2018

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017