BEUDAMED
    34 results · 21ms · Sources: EU EUDAMED, US FDA

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    ONTRAK TESTSTIK FOR METHAMPHETAMINE, CAT. 1986686

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950018123·FORCEP TISSUE GILLIES 1X2 TEETH 6" 15CM

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040043677·Mouth Gag Molt Child

    DEFENDO SINGLE USE VALVE KIT

    FDA UDI
    MEDIVATORS INC.·40677964001367·DEFENDO SINGLE USE VALVE KIT- Cleaning Adapter

    DEFENDO SINGLE USE VALVE KIT

    FDA UDI
    MEDIVATORS INC.·00724995246846·DEFENDO SINGLE USE VALVE KIT- Cleaning Adapter

    Ormesh

    FDA UDI
    ORMCO CORPORATION·00889989017311·ORMESH CURVE LING PAD W/BUTTON

    BARCOMED 5MP2

    FDA 510(k)
    FDA Class 2 ·Radiology

    IMMULITE PHENYTOIN, IMMULITE 2000 PHENYTOIN, CATALOG # LKPN1, LKPN5 & L2KPN2, L2KPN6

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    6000096-1999-00080

    FDA Adverse Event
    Malfunction ·December 22, 1999

    6000096-1999-00079

    FDA Adverse Event
    Malfunction ·December 22, 1999

    6000096-1999-00082

    FDA Adverse Event
    Malfunction ·December 30, 1999

    6000096-1999-00083

    FDA Adverse Event
    Other ·December 30, 1999

    6000096-1999-00078

    FDA Adverse Event
    Malfunction ·December 22, 1999

    6000096-1999-00081

    FDA Adverse Event
    Malfunction ·December 22, 1999

    Defendo Single Use Cleaning Adapter for Olympus Endoscopes (100322, 100323, 4000096, 4003269, 4003280)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    T:SLIM X2 INSULIN PUMP

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code LZG·December 8, 2016

    SMR GLENOSPHERE Ø 36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code MBF·January 4, 2023

    SITTER ELITE

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·February 8, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·February 18, 2011

    VAPR HOOK ELECTRODE

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code GEI·February 1, 2008