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

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    Premier Sealant

    FDA 510(k)
    FDA Class 2 ·Dental

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108161·CASTROVIEJO NEEDLE HOLDER CVD W/ LOCK

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122261·Kwire .062x6" (1.6x150mm) Threaded

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122278·KWire .062x6" (1.6x150mm)

    ECLIPSE WAX REMOVER

    FDA 510(k)
    FDA Class 2 ·Dental

    NEV'S INK AUTOCLAVE TAPES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STERIS

    FDA Adverse Event
    Malfunction ·VILEX·Product code HTY·April 6, 2005

    BD BBL¿ LOWENSTEIN-JENSEN MEDIUM SLANTS 100 EA.

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code KZI·December 28, 2021

    VITALITY

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 14, 2011

    LOGIC

    FDA Adverse Event
    Injury ·OSTEOMED·Product code MQN·May 7, 2013

    ENDO DISSECT* 5MM INSTRUMENT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC·Product code GET·July 23, 2014

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 15, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 11, 2017

    G8

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC, INC.·Product code PDJ·August 27, 2025