BEUDAMED
    22 results · 22ms · Sources: EU EUDAMED, US FDA

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    CMI IMPLANT IS II ACTIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707009405·CALIBRA 1ST MOLAR BANDS n.UR 3

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319703878·DeBakey Atraumatic Tissue Forceps, 2.5mm wide t...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450299036·

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857554382·Anti Torque Alignment Tube Size 105°

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197034500·Standard operating scissors 14,5 c...

    AED

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657017893·Wide Jaw Punch large 3.5mm 15 degree up

    AIRSTRIP REMOTE PATIENT MONITORING (RPM)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PULPDENT COPAL VARNISH WITH FLUORIDE

    FDA 510(k)
    FDA Class 2 ·Dental

    ULTRASEAL

    FDA Adverse Event
    Malfunction ·AMBU A/S·Product code BYG·May 9, 2013

    GOBED II

    FDA Adverse Event
    STRYKER MEDICAL·Product code FNL·May 26, 2011

    TUBE, GASTROINTESTINAL (AND ACCESS)

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code KNT·August 14, 2008

    CONTEGRA PULMONARY VALVED CONDUIT - SUPPORTED

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·June 25, 2014

    T-HANDLE INSERTER

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·April 29, 2021

    REPLACEMENT HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·December 23, 2013

    BD LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·May 4, 2020

    T-HANDLE

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code LXH·May 2, 2023

    IMPLANT INSERTER SH CONNECTION

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·May 2, 2023

    KING LAD SILI CONE SINGLE USE, King Systems devices/case, ETO Sterile. Size 2 / Infant Silicone King LAD¿ Patient Size: 10-20kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012

    Multidiagnost 97

    FDA Recall
    Terminated ·Philips Medical Systems·Product code IZZ·February 20, 2002