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

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    MEDLINE DISPOSABLE VAGINAL SPECULUM

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

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496072942·STRIPE GAME DEMETRA, SIZE XXL, NERO, GRADUATED ...

    THE V BAG, CATALOG NUMBER VB1800; VAC-BOX FOR VACUUM ASSISTED VENOUS DRAINAGE, CATALOG NUMBER VACBOX1500

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PHILIPS EASY VISION FAMILY WORKSTATION OPTION CARDIRAC SCORING

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2017

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·March 12, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 23, 2013

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 2, 2011

    CAPSUREFIX NOVUS

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

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·February 13, 2020

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018