BEUDAMED
    13 results · 24ms · Sources: EU EUDAMED, US FDA

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    EPINEPHRINE REAGENT, CAT. NO. 5367

    FDA 510(k)
    FDA Class 2 ·Hematology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756372114·CCOCC PROCEDURE PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112342·SURG-I-BAND ORANGE GLOW

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112311·SURG-I-BAND BLUE

    CT SPACER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FAVO S-TLIF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PORTEX

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC·Product code JOH·August 21, 2019

    PORTEX

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC·Product code JOH·August 21, 2019

    PORTEX® PORTEX® ULTRAPERC® SINGLE DILATOR KIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code JOH·February 22, 2019

    SCREW-IN

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·November 30, 2010

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 2, 2014

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·July 16, 2020