BEUDAMED
    20 results · 22ms · Sources: EU EUDAMED, US FDA

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    Instru-Safe Instrument Protection System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100158·KRATZ-BARRAQUER SPECULUM LARGE

    Symmetry Surgical Ultra®

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482055557·Ultra Instruments Clamp; Bulldog Vein Clamp; Li...

    SunMed

    FDA UDI
    SUNMED, LLC·20889483000455·CC GUEDEL A/W SZ 40mm BX/50

    Healing Abutment

    FDA UDI
    BICON, LLC·00813110021113·5.0 x 6.0mm Healing Abutment - 2.0mm Post

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171029182·PESSARY, RING #6, W/O SUPPORT, 3.25"

    ASCENT F-COAT MODEL: 006-00097

    FDA 510(k)
    FDA Class 2 ·Dental

    UCP RAPID DRUG SCREENING TESTS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Bespa Charcot System

    FDA UDI
    Kapstone Manufacturing, LLC·00810041320513·Seg Column, Screw, 40

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962111062·BULLDOG VEIN CLAMP, 1 1/2", SLIGTHLY CVD, TITANIUM

    Widex

    FDA UDI
    Widex A/S·05706069887785·WIDEX MOMENT M-IM (Clay brown ) 440, Left

    Widex

    FDA UDI
    Widex A/S·05706069655681·Widex UNIQUE U-IM (Clay brown ) 440, Left

    Widex

    FDA UDI
    Widex A/S·05706069655698·Widex UNIQUE U-IM (Dark brown ) 440, Left

    Widex

    FDA UDI
    Widex A/S·05706069887792·WIDEX MOMENT M-IM (Dark brown ) 440, Left

    Widex

    FDA UDI
    Widex A/S·05706069655674·Widex UNIQUE U-IM (Light beige ) 440, Left

    Widex

    FDA UDI
    Widex A/S·05706069887778·WIDEX MOMENT M-IM (Light beige ) 440, Left

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 6, 2013

    NA

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·June 22, 2011

    KUGEL PATCH

    FDA Adverse Event
    Injury ·DACOL INC., SUB. C.R. BARD, INC.·Product code FTL·September 3, 2008

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 24, 2015