BEUDAMED
    8,946 results · 38ms · 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 ×

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·September 22, 2025

    TOTAL ASR FEM IMP SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KXA·July 2, 2014

    ASR ACETABULAR IMPLANT 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 2, 2014

    Prosthesis, Hip, Hemi-, Acetabular, Cemented, Metal

    FDA classification
    FDA Class 3 ·Prosthesis, Hip, Hemi-, Acetabular, Cemented, Metal

    DUROM US ACETABULAR COMPONENT 56/50 P

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWB·March 20, 2012

    LATERAL STRAIGHT STEM 15.0 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·March 28, 2012

    DUROM US ACETABULAR COMPONENT 56/50 P

    FDA Adverse Event
    Injury ·ZIMMER INC.·Product code KWB·March 6, 2012

    UNKNOWN DEPUY SROM 28, 10 DEGREE LINER

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code KWB·March 29, 2012

    UNKNOWN DEPUY 56+4 DURALOC LINER

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code KWB·March 6, 2012

    UNKNOWN PSL-HA CLUSTER ACETABULAR SHELL

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code KWB·January 24, 2012

    DUROM US ACETABULAR COMPONENT 50/44 J

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWB·March 28, 2012

    UNKNOWN DEPUY 28 10 DEGREE LINER

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code KWB·March 14, 2012

    DUROM US ACETABULAR COMPONENT 56/50 P

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWB·March 3, 2012

    MONOBLOCK ACETABULAR CUP

    FDA Adverse Event
    Injury ·ZIMMER TMT·Product code KWB·January 16, 2009

    UNKNOWN DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·February 19, 2009

    UNKNOWN DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·February 20, 2009

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD., U.K.·Product code KWB·February 12, 2009

    UNKNOWN DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·January 9, 2009

    UNKNOWN DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·February 16, 2009

    UNKNOWN DEPUY CUP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·January 9, 2009