BEUDAMED
    8 results · 20ms · 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 ×

    FerriSmart Analysis System

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYRINGE 1ML 29G 12.7MM 10BAG 500 EU

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·November 2, 2020

    MAX ADJUSTING INSTRUMENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    COMPACT PIEZO P2K, POWERCARE

    FDA 510(k)
    FDA Class 2 ·Dental

    QUATTRODE 30-CM LENGTH PERCUTANEOUS LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 7, 2011

    QUICKSITE LV

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. CRMD·Product code OJX·January 13, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 21, 2013

    SYRINGE 1ML 29G 12.7MM 10BAG 500 EU

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·July 30, 2020