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

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    OMEGA LABORATORIES HAIR DRUG SCREENING ASSAY PHENCYCLIDINE

    FDA 510(k)
    FDA Unclassified ·Unknown

    kitazato IUI Catheter

    FDA UDI
    KITAZATO CORPORATION·04580303269237·Catheter with Outer Stiffener with Stainless St...

    3.5MM CORTEX SCREW SELF-TAPPING 55MM

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HWC·January 26, 2017

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·July 25, 2018

    BEL-CAT

    FDA 510(k)
    FDA Class 2 ·Radiology

    EXTERNAL FIXATION SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 18, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018

    QUANTA SYSTEM S.P.A.

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·July 10, 2015

    3.5MM CORTEX SCREW SELF-TAPPING 16MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 6, 2016

    3.5MM CORTEX SCREW SELF-TAPPING 14MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 6, 2016

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code ITI·October 1, 2014

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011

    DECKER FCP 1.5X5MM CUP UP

    FDA Adverse Event
    Malfunction ·Product code HTX·July 18, 2008

    CLEARVIEW UTERINE MANIPULATOR

    FDA Adverse Event
    Injury ·CLINICAL INNOVATIONS, LLC·Product code LKF·June 11, 2024

    Pain Tray Catalog Number: 9883

    FDA Enforcement
    Class II ·Terminated·Busse Hospital Disposables, Inc.·June 8, 2022

    CORTSCR 3.5 SELF-TAP L65 TI

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·April 29, 2013

    3.5MM CORTEX SCREW SELF-TAPPING 22MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 21, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·January 4, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 14, 2016