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

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    NEXUS I.V. NEEDLESS ACCESS CANNULA FOR INTRAVASCULAR ADMINISTRATION SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517283849·CoRoent® Large MP, 11x9x23 8°

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014609713·MAQUET 2" SOFTCARE

    EVOLIS 3031.0003 CEMENTLESS TIBIAL BASEPLATE SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 22, 2023

    KURZ UPPER EYELID IMPLANT SIZERS, MODEL 8000 111

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BACT/ALERT SN CULTURE BOTTLE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 31, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 29, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·January 14, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·April 13, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·September 9, 2011

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 14, 2011

    EVOLIS STD FEMUR TI PLASMA SPRAYED RIGHT SIZE 4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2019

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·February 21, 2014

    RESTORE SENSOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 26, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·April 14, 2011

    WIRE GUIDE

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DQX·July 3, 2008

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    BACT/ALERT I NST 100 BTLS - 259785

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX INC.·Product code MDB·March 4, 2024