BEUDAMED
    14 results · 19ms · 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 ×

    MAXIM KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993159·anteriors; shade A4; mould UIM

    PR CREAM

    FDA 510(k)
    FDA Unclassified ·Unknown

    NeuroAmp II, NeuroAmp II.5s

    FDA 510(k)
    FDA Class 2 ·Neurology

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·March 7, 2013

    PLM A+3 MEDNET WRLSS

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·January 18, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    DURAL ALPHA INSERT W RIM II/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·March 12, 2019

    DURASUL, ALPHA INSERT, HOODED, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·September 28, 2018

    METASUL, ALPHA INSERT, JJ/28

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·February 4, 2019

    DURASUL, ALPHA INSERT, KK/36

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·March 13, 2018

    COCR HEAD 32/ 0 'M' 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·June 4, 2019

    DURASUL, ALPHA INSERT, LL/36

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·April 29, 2019

    DURASUL, ALPHA INSERT, HOODED, KK/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·June 15, 2018