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

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    IMMUNALYSIS BUPRENORPHINE URINE ENZYME IMMUNOASSAY, IMMUNALYSIS BUPRENORPHINE URINE CONTROLS AND CALIBRATORS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Oticon

    FDA UDI
    Oticon A/S·05707131271396·NERA, KIT 10 WL OMNI 85 BE

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221037312·Unitek(TM) Bicuspid Band General Purpose Wide L...

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321414060·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311414060·

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857581012·Split Tube Retractor Ø12x80 mm

    NEWPORT C250 AIR COMPRESSOR MODEL C250

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072006894·HIGH VACUUM SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072006900·HIGH VACUUM SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072006931·HIGH VACUUM SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072006917·HIGH VACUUM SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072006924·HIGH VACUUM SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072006948·HIGH VACUUM SUCTION REGULATORS

    INCLUSIVE TAPERED IMPLANT

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 17, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 4, 2014

    SCRDRIVERSHAFT T25 F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·June 3, 2013

    CUB PEDIATRIC CRIB-FIXED BASE

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FMS·June 1, 2011

    Medtronic Intrathecal Catheter, Model 8731, (part of infusion systems using Medtronic implantable pumps) The catheter is designed for use in the intrathecal space. Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA.

    FDA Recall
    Terminated ·Medtronic Neurological·Product code LKK·July 21, 2006