BEUDAMED
    682 results · 25ms · Sources: EU EUDAMED, US FDA

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    WONDFO AMPHETAMINE URINE TEST, WONDFO BARBITURATES URINE TEST, WONDFO BENZODIAZEPINES URINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169601635·SPACER 2111560 OLIF25 20MM 6 DEG 16X60

    MOVES

    FDA UDI
    Thornhill Research Inc·10807141000077·ASSY, MOVES System Case

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486017309·MCK CALIPER

    NA

    FDA UDI
    Smith & Nephew, Inc.·03596010039392·FEMORAL PROSTHESIS DRIVER

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317300706·

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10885380077357·1.1mm Non-Threaded Guide Wire 150mm

    OptumSI Implant System

    FDA UDI
    SI Solutions, LLC·00850057247237·Sacroiliac Joint Fusion Implant, 11.5mm x 60mm

    MicroSelectron Digital

    FDA UDI
    Nucletron B.V.·08717213033917·Coupling Treatment Tube for 5F Flexibles (28)

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122223·KWire .045x6" (1.1x150mm)

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122216·KWire .045x6" (1.1x150mm) Threaded

    TRUBYTE DENTURE BASE RESIN SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDLINE RETRACTABLE SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 14, 2013

    AML/TL ENDR REP LINER 32X54SP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·May 13, 2011

    ITREL 3

    FDA Adverse Event
    Injury ·MEDTRONIC SWISS MANUFACTURING FACILITY·Product code LGW·August 13, 2008

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026