BEUDAMED
    9 results · 21ms · 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 ×

    XE CHECK

    FDA 510(k)
    FDA Class 2 ·Hematology

    POINTER F-3 TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    ZIMMER TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·March 8, 2013

    VASOVIEW HEMOPRO EVH SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·January 14, 2011

    S-ROM*SLEEVE PRX ZTT, 20F-XXL

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code LPH·August 8, 2014

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 22, 2014

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 15, 2015

    SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·November 25, 2014