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.

    IMAGEVIEW 46000

    FDA 510(k)
    FDA Class 2 ·Radiology

    620 FLUOROSCOPIC TABLE, TILT OR POWER MEDICAL TAB

    FDA 510(k)
    FDA Class 2 ·Radiology

    CDI(TM) H/S CUVETTE, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIGITALDIAGNOST DUAL DETECTOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS DMC GMBH·Product code MQB·January 17, 2013

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    3.0MM TI STERNAL LCKNG SCREW SELF-DRILLING/10MM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·July 10, 2014

    ENDURITY Pulse Generator REF PM**** SN ********* St. Jude Medical Cardiac Rhythm Assurity and Endurity pacemakers are intended to provide single-chamber or dual-chamber bradycardia pacing.

    FDA Enforcement
    Class I ·Ongoing·St. Jude Medical, Cardian Rhythm Management Division·May 19, 2021