BEUDAMED
    86 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    MAXENON XI 300-WATT XENON LIGHT SOURCE

    FDA Adverse Event
    Injury ·QED, INC·Product code FST·January 16, 2014

    MAXENON XI 300-WATT XENON LIGHT SOURCE

    FDA Adverse Event
    Injury ·QED, INC·Product code FST·September 16, 2013

    MAXENON XI 300-WATT XENON LIGHT SOURCE

    FDA Adverse Event
    Injury ·QED, INC·Product code GCT·September 16, 2013

    MAXENON XI 300-WATT XENON LIGHT SOURCE

    FDA Adverse Event
    Injury ·QED, INC·Product code FST·September 16, 2013

    AED, INC.

    FDA Adverse Event
    Injury ·AES, INC.·Product code CAE·May 30, 2014

    STEFFE PEDICLE SCREW

    FDA Adverse Event
    Injury ·MICRO MED, INC.·Product code MCV·June 13, 1995

    BOSTON SCIENTIFIC SCI-MED INC

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQX·September 4, 2002

    BRASSELER TRITON ALL IN ONE IRRIGATION SOLUTION

    FDA Adverse Event
    Injury ·INTER-MED, INC.·Product code KJJ·April 28, 2025

    PIPELINE FLEX EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code OUT·March 16, 2020

    STERI MED, INC ETHICON TROCAR BLUNT TIP ENDOPATH XCEL

    FDA Adverse Event
    Injury ·STERILE MED REPROCESSOR·Product code GCJ·October 14, 2009

    GDLH

    FDA Adverse Event
    Injury ·DANEK MED. INC.·Product code MNH·May 17, 2000

    BBRAUN OUTLOOK 400ES 621-400ES

    FDA Adverse Event
    Injury ·BBRAUN MED, INC·Product code FRN·September 7, 2011

    ANGIOJET ULTRA SYSTEM

    FDA Adverse Event
    Injury ·POSSIS MED, INC.·Product code MCX·June 30, 2009

    CELSITE

    FDA Adverse Event
    Injury ·B.BRAUN MED INC.·Product code LJT·October 12, 2000

    ABBOTT

    FDA Adverse Event
    Injury ·ICU MED INC.·Product code FPA·September 13, 1997

    TOURNI-COT - UNIVERSAL

    FDA Adverse Event
    Injury ·MAR-MED INC.·Product code GAX·November 5, 2020

    STRYKER COLORADO ELECTRODE

    FDA Adverse Event
    Injury ·STERILE MED, INC.·Product code GEI·September 22, 2011

    MINI MED

    FDA Adverse Event
    Injury ·MINI MED INC·Product code LZG·December 11, 2000

    CUSTOM ARTHROGRAM TRAY

    FDA Adverse Event
    Injury ·NI-MED, INC.·Product code KDD·April 27, 1995

    VISTA DENTAL PRODUCTS / SYRINGE SODIUM HYPOCHLORITE

    FDA Adverse Event
    Injury ·INTER - MED, INC.·Product code KJJ·May 22, 2019