BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    UBI MAGIWEL FERRITIN QUANTITATIVE

    FDA 510(k)
    FDA Class 2 ·Immunology

    LMA FASTRACH ETT SINGLE USE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Panther Fusion GI Expanded Bacterial Assay

    FDA 510(k)
    FDA Class 2 ·Microbiology

    UNKNOWN OXFORD MENISCAL KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code NRA·October 17, 2017

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code NIK·February 9, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·January 4, 2011

    SUMMIT DUOFIX TAP SZ7 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·July 23, 2014