BEUDAMED
    452 results · 47ms · Sources: EU EUDAMED, US FDA

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    SRI SURGICAL

    FDA Adverse Event
    Malfunction ·SRI SURGICAL·Product code GCJ·May 14, 2010

    CLOSURE TAPE USED TO SECURE VAG DELIVERY PACK

    FDA Adverse Event
    Other ·SRI SURGICAL·Product code FRG·August 14, 2008

    VISTEC SPG 4X8 NON ST 10S 16PLY

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/ KENDALL·Product code FRO·September 15, 2006

    SRI SURGICAL BREAST PACK

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

    SRI/SURGICAL EXPRESS, INC

    FDA Adverse Event
    Malfunction ·SRI/SURGICAL EXPRESS, INC.·Product code FYB·January 6, 2005

    STERILE PUMP PACK

    FDA Adverse Event
    Malfunction ·SRI SURGICAL·Product code FSM·July 2, 2011

    MONOPOLAR HANDLE WITH L-HOOK

    FDA Adverse Event
    Malfunction ·SRI SURGICAL·Product code GEI·June 5, 2006

    STERILE PACK OF TOWELS; 8 TOWEL PK (FF)

    FDA Adverse Event
    Malfunction ·SRI SURGICAL·Product code KKX·May 30, 2011

    BURN SKIN STAPLER FROM STERILE BARCODE BURN PACK

    FDA Adverse Event
    Malfunction ·SRI SURGICAL·Product code FSM·July 29, 2012

    SRI LIQUID PROOF SURGICAL GOWN

    FDA Adverse Event
    Malfunction ·SRI/SURGICAL EXPRESS, INC.·Product code FYB·February 18, 2004

    STERILE STANDARD GOWN

    FDA Adverse Event
    Malfunction ·STERILE RECOVERIES, INC.·Product code FYA·October 21, 1997

    UNK BROACH

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code HTQ·November 7, 2024

    MICROPOWER OSCILLATOR SAW, DETACHABLE LEVER

    FDA Adverse Event
    Malfunction ·CONMED LINVATEC·Product code HWE·December 14, 2007

    MICROPOWER OSCILLATOR SAW, DETACHABLE LEVER

    FDA Adverse Event
    Malfunction ·CONMED LINVATEC·Product code HWE·December 14, 2007

    RAYTEC

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code GDY·May 8, 2013

    SRI-SURGICAL STERILE PACK ANGIO CATH LAB

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code KDD·March 31, 2016

    UNK INSERTION DEVICE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWE·June 12, 2024

    WELLINGTON LAP

    FDA Adverse Event
    Malfunction ·SRI/ SURGICAL EXPRESS, INC.·Product code GCJ·September 15, 2011

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    FDA Adverse Event
    SRI/SURGICAL EXPRESS, INC.·Product code EFQ·February 10, 2010

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    FDA Adverse Event
    Malfunction ·SRI/SURGICAL EXPRESS, INC.·Product code FFZ·April 11, 2005