BEUDAMED
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    ARX SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Dila-Cath Nelaton 40cm CH16

    FDA UDI
    Wellspect AB·07333387040936·Urinary catheter for intermittent dilatation

    Dila-Cath Nelaton 40cm CH16

    FDA UDI
    Wellspect AB·07392532131707·Urinary catheter for intermittent dilatation

    JOBST Confidence

    FDA UDI
    BSN-Jobst GmbH·04059993452491·CONFIDENCE 3/THIGH HIGH/SLANT-CLOSED TOE/DOTTED...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702581508·Elvarex 1/Knee High/Slant-Closed Toe/SoftFit-Sl...

    JOBST Confidence

    FDA UDI
    BSN-Jobst GmbH·04059993442478·CONFIDENCE 2/THIGH HIGH/SLANT-CLOSED TOE/DOTTED...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702250169·ELVAREX 2/THIGH HIGH/SLANT-OPEN TOE-ELEPHANTIAS...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702450101·ELVAREX 2/KNEE HIGH/SLANT-CLOSED TOE-ELEPHANTIA...

    JOBST Confidence

    FDA UDI
    BSN-Jobst GmbH·04059993472239·CONFIDENCE 1/THIGH HIGH/SLANT-CLOSED TOE/DOTTED...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702361094·Elvarex 3/Chap Style/Open Toe-Elephantiasis-Ver...

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K0606000·Tray, Base, 6"

    DL950 Braemar

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146DL95000·

    <GENX> CODA INCUBATOR CELLMATE

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

    CONDUCTION CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·September 8, 2015

    REFURB, 3RD ED., C/U, S&N DYONICS 25

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code HRX·December 27, 2016

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·April 16, 2013

    CE MULTIRATE INFUSOR LV2,3,512 PACK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·April 18, 2011

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·June 17, 2008

    LEAD EXTRACTION EVOLUTION SHORTIE RL CONTROLLED-ROTATION DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·September 9, 2015