BEUDAMED
    7,011 results · 40ms · 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 ×

    PUMP CURLIN 6000CMS

    FDA Adverse Event
    Malfunction ·MOOG / ZEVEX, INC.·Product code FRN·July 8, 2024

    RESTYLANE KYSSE

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LMH·November 6, 2024

    UNKNOWN HIP FEMORAL AUGMENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·November 22, 2019

    UNK ELITE HYL CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWY·March 14, 2002

    UNK HYL HIP LNR

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·July 3, 2003

    UNK HYL HIP LNR

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·September 9, 2003

    UNK HYL HIP LNR

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·August 20, 2003

    UNK HYL KNEE INS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·April 15, 2003

    UNK HYL KNEE INS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·April 15, 2003

    DURALOC 28MM NEUT HYL GP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·July 18, 2005

    GLOBAL SHD HYL PEG GLENOID 48

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code KWS·January 6, 2012

    GLOBAL SHD HYL PEG GLENOID 44

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HRY·February 26, 2010

    AML/TL HYL REP LINER 32X44SP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 14, 2004

    AML/TL HYL REP LINER 32X50SP

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code JDI·May 30, 2012

    GLOBAL SHD HYL PEG GLENOID 52

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code KWY·May 29, 2012

    GLOBAL SHD HYL FIN GLENOID 44

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWS·January 9, 2002

    GLOBAL SHD HYL FIN GLENOID 44

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWS·March 6, 2002

    GLOBAL SHD HYL PEG GLENOID 48

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWS·February 14, 2002

    GLOBAL SHD HYL FIN GLENOID 52

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWS·March 27, 2002

    GLOBAL SHD HYL FIN GLENOID 44

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWS·March 6, 2002