BEUDAMED
    6 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 ×

    CONMED ELECTROSURGICAL GROUNDING PAD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    JACKSON RARE EARTH MAGNETIC ATTACHMENT

    FDA 510(k)
    FDA Class 1 ·Dental

    SPIROLOOP, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CAPSUREFIXNOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 11, 2013

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 10, 2011

    HT70 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·July 11, 2014