BEUDAMED
    7 results · 25ms · 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 FDA Adverse Event ×

    CER OPTION TYPE 1 TPR SLEVE -3

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 7, 2018

    EPOLY 32MM RLC LNR MROM SZ23

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 7, 2018

    CER BIOLOXD OPTION HD 32MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 7, 2018

    M/H SLD/APX HLE RNGLC SHL 50MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 7, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 15, 2014

    PROTECTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code LWS·October 31, 2012

    PROXIMATE*ILS CURVED CIR STAPL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 23, 2010