BEUDAMED
    26 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ADVANCE(R) DURAMER(R) REVISION CCK INSERT

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·January 29, 2019

    CLARITI TORIC FRP (SOMOFILCON A)

    FDA Adverse Event
    Injury ·COOPERVISION CL LIMITED·Product code LPL·July 26, 2017

    CLARITI TORIC FRP (SOMOFILCON A)

    FDA Adverse Event
    Injury ·COOPERVISION CL LIMITED·Product code LPL·July 26, 2017

    CLARITI MULTIFOCAL FRP (SOMOFILCON A)

    FDA Adverse Event
    Injury ·COOPERVISION CL LIMITED·Product code LPL·April 13, 2017

    CLARITI ELITE FRP (SOMOFILCON A)

    FDA Adverse Event
    Injury ·COOPERVISION MANUFACTURING LTD·Product code LPL·June 15, 2018

    CLARITI ELITE FRP (SOMOFILCON A)

    FDA Adverse Event
    Injury ·COOPERVISION MANUFACTURING LTD·Product code LPL·June 15, 2018

    CLARITI XR TORIC (FRP) (SOMOFILCON A)

    FDA Adverse Event
    Injury ·COOPERVISION MANUFACTURING LTD·Product code LPL·March 29, 2019

    965 MICRO VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Injury ·IMED CORPORATION, SAN DIEGO, CA 92131·Product code FRN·July 29, 1992

    TARRY MANUFACTURING

    FDA Adverse Event
    Injury ·TARRY MANUFACTURING·Product code FRP·September 24, 2009

    BENDY BUMPER

    FDA Adverse Event
    Injury ·CHILDREN'S MEDICAL VENTURES, INC.·Product code FRP·October 22, 1999

    FRP 316 VARIABLE ANGLE LOCKING SCREW, D:3.5MM X L:16.0MM

    FDA Adverse Event
    Injury ·FLOWER ORTHOPEDICS·Product code HWC·June 5, 2018

    DXTEND GLENOSPHERE STD D38MM

    FDA Adverse Event
    Injury ·FRA·Product code HSD·April 26, 2018

    ARP STIMULATOR

    FDA Adverse Event
    Injury ·ARP MANUFACTURING LL·Product code IPF·April 15, 2008

    UNKNOWN SIGMA 2 RP TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·July 14, 2017

    UNKNOWN DEPUY 2 RP TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 6, 2015

    BLT Ø4.1MM RC, SLA® 8MM, TIZR, LOXIM

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·January 27, 2025

    UNKNOWN DEPUY SZ 2 RP TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·December 30, 2014

    UNKNOWN DEPUY SZ 2 RP TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code JWH·September 26, 2011

    UNKNOWN DEPUY SIGMA SZ 2 RP TIB TRAY

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 5, 2013

    UNKNOWN DEPUY SIGMA SZ 2 RP TIBIAL TRAY

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code NJL·September 2, 2014