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

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    NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR

    FDA 510(k)
    FDA Class 2 ·Neurology

    Mini-Mono®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70606251·Mini-Mono-Brackets Roth 'S2' .022" 9° 1000 Brac...

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K0604250·Tray, Base, 4.25"

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K0602250·Tray, Base, 2.25"

    EUROSPITAL EU-TTG IGA UMANA

    FDA 510(k)
    FDA Class 2 ·Immunology

    SCANDINAVIAN IVF SCIENCES AB, G1.2

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

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 27, 2013

    SHILEY LPC

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTO·June 13, 2008

    DEPUY ASR FEM IMPLANT SZ 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·April 6, 2011

    BD VACUTAINER® LH PST¿ II PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·July 25, 2018

    UNKNOWN BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·March 10, 2017