BEUDAMED
    404 results · 38ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    SRI SURGICAL BREAST PACK

    FDA Adverse Event
    Injury ·SRI SURGICAL·Product code LRP·May 24, 2006

    MERSILENE POLYESTER FIBER SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·December 20, 2017

    UNKNOWN SPACEMAKER BALLOON

    FDA Adverse Event
    Injury ·US SURGICAL PUERTO RICO·Product code GCJ·January 28, 2022

    UNKNOWN LIGASURE INSTRUMENT

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 21, 2020

    MERSILENE POLYESTER FIBER SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·December 14, 2017

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·September 21, 2021

    VICRYL PLUS POLYGLACTIN 910 SUTURE UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·September 21, 2021

    UNKNOWN CUSA EXCEL

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·May 11, 2018

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·July 31, 2019

    SIGMA HP UNI FEMORAL SZ2 RM/LL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NPJ·September 4, 2025

    HP UNI INS SZ2 7MM RMLL AOX

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code HRY·September 4, 2025

    UNKNOWN PROGRIP MESH PRODUCT

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·September 18, 2023

    S4 SET SCREW NEW VERSION

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code MNI·February 12, 2020

    S4 SET SCREW NEW VERSION

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code MNI·February 12, 2020

    PENTA 3MM LEAD, 60 CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·September 30, 2022

    SILASTIC MAMMARY IMPLANT, LPR, NFP

    FDA Adverse Event
    Injury ·DOW CORNING CORP.·Product code FTR·February 5, 1998

    SILICONE BREAST IMPLANT

    FDA Adverse Event
    Injury ·DOW CORNING CORP./MDR REPORTING & COMPLAINT INVESTIGATION·Product code FTR·December 31, 1997

    DOW CORNING

    FDA Adverse Event
    Injury ·DOW CORNING·Product code FTR·December 22, 2007

    INOGEN MINI ICD VR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·September 23, 2019

    PROCLAIM 5 ELITE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·September 27, 2019