BEUDAMED
    418 results · 37ms · Sources: EU EUDAMED, US FDA

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    VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139243387·UNITY KNEE™ PS-C INSERT - Size 1 x 18mm

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780376965·Integra® Jarit® Webster Needle Holder, 4-1/2", ...

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113058·PS Insert, Size 1 x 18mm

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319739419·Adson Dressing Forceps 4-3/4" (11.9cm), serrate...

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973100706·Poly Insert UCCS, Size 1, 18mm

    STIMTRODE SINGLE USE NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SNORE GUARD ADVANCE

    FDA 510(k)
    FDA Class 2 ·Dental

    Widex

    FDA UDI
    Widex A/S·05706069972030·WIDEX MOMENT MBB2 220 (Tech black)

    Widex

    FDA UDI
    Widex A/S·05706069794434·Widex EVOKE E-FP (Tech Black ) 220, Telecoil, V...

    Widex

    FDA UDI
    Widex A/S·05706069806304·Widex EVOKE E-FA (Tech Black ) 220, Telecoil, V...

    Widex

    FDA UDI
    Widex A/S·05706069923230·WIDEX MOMENT MBB3D 220 (Tech black)

    Widex

    FDA UDI
    Widex A/S·05706069807349·Widex EVOKE E-FM (Tech Black ) 220, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069884326·WIDEX MOMENT MRR2D (Tech Black ) 220, RC coil, ...

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 25, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 26, 2011

    EPOC HOST

    FDA Adverse Event
    Malfunction ·EPOCAL INC.·Product code CGL·October 5, 2020

    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