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

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    HELICAL RIDGE PEEK INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RTA MODEL D RETINAL THICKNESS ANALYZER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PIEZO BONE SURGERY

    FDA 510(k)
    FDA Class 2 ·Dental

    KOTEX NATURAL BALANCE : TAMPON, MENSTRUAL, UNSCENTED : HEB

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK CORPORATION CONWAY MILL·Product code HEB·June 21, 2018

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 3, 2013

    OSCILL-SAW-ATTACHM F/532.001 532.010 532

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·October 3, 2014

    ASR ACETABULAR IMPLANT 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·June 22, 2011

    COBALT HV W/ GENTAMICIN POWDER BONE CEMENT 40 GRAMS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·October 2, 2017

    COBALT HV W/ GENTAMICIN POWDER BONE CEMENT 40 GRAMS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·October 6, 2017

    ONCOLOGY SALVAGE SYSTEM

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

    ONCOLOGY SALVAGE SYSTEM

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

    INTELLIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·November 20, 2019

    INTELLIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·April 12, 2021