BEUDAMED
    33 results · 24ms · Sources: EU EUDAMED, US FDA

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    LEAK DETECTION SENSOR AND TRAY ACCESSORY KIT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Phasor Drill

    FDA UDI
    BIOTEX, INC.·M710PH580700·2 Flute Drill Bit.

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014609157·SKYTRON 3" DELUXE

    CD22-APC

    FDA UDI
    Miltenyi Biotec B.V. & Co. KG·04049934134166·Clone REA340 recognizes the human CD22 antigen,...

    EVOLIS 3031.0003 CEMENTLESS TIBIAL BASEPLATE SIZE 3

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

    OSMETECH MICROBIAL ANALYSER-URINARY TRACT INFECTION DETECTOR (OMA-UTI)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    KAWASUMI LABORATORY BLOOD DRAWING KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    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

    SYSTEM 6 ASEPTIC HOUSING ASSY

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code KIJ·April 26, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·April 14, 2011

    LIFEPAK 9P DEFIBRILLATOR/MONITOR/PACEMAKER

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·July 18, 2008

    BD PRESET¿ ECLIPSE¿

    FDA Adverse Event
    Injury ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 17, 2024

    BD PRESET¿ ECLIPSE¿

    FDA Adverse Event
    Injury ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 17, 2024