BEUDAMED
    31 results · 25ms · Sources: EU EUDAMED, US FDA

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    DAR-9400F

    FDA 510(k)
    FDA Class 2 ·Radiology

    Cook

    FDA UDI
    COOK INCORPORATED·00827002141339·Fascial Dilator

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0730060·Rod Bender, 5.5 mm, 5 Position

    Driver Pin

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215057145·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197175203·Coakley Curettes Fig. 6 170mm,...

    Genius Total Knee System

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215022891·

    LIFESHIELD ADDITIVE PIERCING PIN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDICAL DEPOT POWER NEB 1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Crescendo Meniscal Insert PS 10mm Size 6

    FDA UDI
    AMPLITUDE SAS·03701089525060·

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 15, 2024

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·July 2, 2020

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 22, 2013

    IN TOUCH ZX

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·April 19, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·July 7, 2020

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·December 13, 2022

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·March 17, 2010

    BD EMERALD¿ 10ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·November 7, 2017

    ARCHITECT C8000

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC·Product code JJE·January 23, 2008

    Conmed System 2500 Electrosurgical Unit, REF 60-8011-SYS, Conmed Corporation

    FDA Recall
    Terminated ·Conmed Electrosurgery·Product code GEI·September 5, 2006