BEUDAMED
    68 results · 23ms · Sources: EU EUDAMED, US FDA

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    SPECTRA OPTIA R APHERESIS SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317328878·

    DIAMOND WORKHORSE SCREW™, Ø3.5mm x 90mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665038484·

    BONE CUTTER/NAIL NIPPER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896051362·BONE CUTTER/NAIL NIPPER DOUBLE ACTION BARREL SP...

    APK

    FDA UDI
    APK Technology Co.,Ltd.·06946725513460·Datex Ohmeda Compatible Short SpO2 Sensor, Pedi...

    Orthopaedic Surgical Instruments

    FDA UDI
    CITIEFFE SRL·08056711921266·

    SOPRO 67D OPERATING ROOM CAMERA

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

    MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 1 ·Dental

    TAPERLOC COMPLETE PRIMARY FEMORAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·August 20, 2018

    TAPERLOC COMPLETE PRIMARY FEMORAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·August 20, 2018

    TAPERLOC COMPLETE PRIMARY FEMORAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·August 20, 2018

    TAPERLOC COMPLETE PRIMARY FEMORAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·August 20, 2018

    TAPERLOC COMPLETE PRIMARY FEMORAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·August 20, 2018

    COOLRAIL LINEAR PEN

    FDA Adverse Event
    Injury ·ATRICURE, INC.·Product code OCL·December 31, 2020

    SYNCHRON DRUG CALIBRATOR 1

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DKB·April 26, 2012

    GALAXY INTRAVASCULAR ULTRASOUND SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code IYO·May 9, 2013

    SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 19, 2014

    UNICEL® DXL 800 ACCESS® IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code LGD·May 25, 2011

    E1 RINGLOC ACETABULAR LINER 36MM SIZE 23 +3MAXROM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MAY·October 11, 2016

    G7 DUAL MOBILITY LINER 38MM C

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 12, 2023