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

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    Manual Wheelchair (A006)

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517194107·MaXcess Access Blade, 110mm Left

    Repose 45cm Cushion, Pump, and PU Cover EU

    FDA UDI
    Frontier Therapeutics Inc·05056279301763·Repose 45cm Cushion, Pump, and PU Cover EU

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946061999·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 12 LE...

    X Series

    FDA UDI
    Zoll Medical Corporation·00847946058074·MAIN ASSY, X SERIES ADVANCED MONITOR/DEFIBRILLA...

    DRILL, AO, STERILE 4, 2X340 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 23, 2011

    APEX MODULAR ACETABULAR CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONE STEP SINGLE/MULTI-DRUG TEST CUP; ONE STEP SINGLE SINGLE/MULTI-DRUG TEST DIPCARD

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172368·CR Tibial Insert Trial with Posterior Pin Relie...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101399·R CR E-MAXTM Vitamin E Congruent Tibial Insert ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102167·R CR MAXTM HXL Congruent Tibial Insert Sz A 10mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523165575·R CR Tibial Insert Trial with Anterior Slot, Sz...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523145065·R CR UHMWPE Congruent Tibial Insert Sz A 10mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124404·R CR Tibial Insert Trial Sz A 10mm

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981302313·Lollipop Trial, Anterior-Angled, 23mm x 11mm x ...

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·January 17, 2025

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 11, 2008

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·August 26, 2011

    PLMA DVC V11.51 1 R

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 12, 2013

    CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HWE·April 19, 2026