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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    DURAGEN SECURE DURAL REGNERATION MATRIX

    FDA 510(k)
    FDA Class 2 ·Neurology

    SimPro™ Now

    FDA UDI
    Wellspect AB·07333387032207·Single Use Urinary Catheter with water sachet. ...

    SimPro™ Now

    FDA UDI
    Wellspect AB·07392532188558·Single Use Urinary Catheter with water sachet. ...

    Brava

    FDA UDI
    Coloplast A/S·05708932513630·Brava Lubricating Deodorant / Brava / Brava ...

    M-Flex®

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·00816734020210·Blue Silicone Tungsten Maloney Bougie Set

    NATRELLE Silicone-Filled Breast Implants

    FDA UDI
    Allergan, Inc.·10888628002593·NATRELLE Style 120-600 High profile BIOCELL |te...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702598476·Elvarex 2/Knee High/Profile-Slant-Open Toe-Elep...

    TALOS®-C HA

    FDA UDI
    MEDITECH SPINE, LLC·B167521206000·

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702256024·Elvarex 2/Thigh High/Slant, Open Toe, E-Version...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702932232·ELVAREX FORTE 3/KNEE HIGH/SLANT-CLOSED TOE-ELEP...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702635348·ELVAREX 4/THIGH HIGH/SLANT-OPEN TOE/SLIP FORM ...

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K1106000·Tray, Base, 6", Arcamed

    BLACKSTONE III ANTERIOR CERVICAL PLATING SYSTEM (PLATE WASHER)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROSTHODONTIC SCREWDRIVER , MODEL IA-400

    FDA 510(k)
    FDA Class 1 ·Dental

    PYRAMID

    FDA UDI
    The Wells Johnson Company·B458201206000·Cannula, Pyramid, specify length, diameter, tip...

    BD PARADIGM LINK BLOOD GLUCOSE MONITOR

    FDA Adverse Event
    Other ·BECTON DICKINSON·Product code NBW·January 19, 2006

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code OZO·April 14, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 16, 2025

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·March 25, 2022