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

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    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0103100·Shaver, Closed, 10mm

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345024052·Paddle Shaver, 10mm

    MODIFICATION TO TRIDENT ALL POLY CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Aligned Medical Solutions

    FDA UDI
    Aligned Medical Solutions·B09800103100·Mosquito Curved Forcep

    Endo Carry-on Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964150043·Endo Carry-on Procedure Kit Includes Basin, Spo...

    RESPONDER 5, INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828183109·RESPONDER 5, INTERACTIVE

    Oxygen Sensor

    FDA UDI
    MERCURY ENTERPRISES, INC.·10641043103104·

    Ovation Tribute Hip Stem

    FDA UDI
    Ortho Development Corporation·00822409011032·STD SIZE 10 Stem Plasma Spray

    RESPONDER 5, ENHANCED

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828139397·RESPONDER 5, ENHANCED

    AFCS PEARLS™ Extension Hose

    FDA UDI
    Synergie Nederland B.V.·08720387388028·Air-Fluidized bed - see www.synergiecare.com E...

    Soft-Form™ ALD External Nasal Splint

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501022519·Soft-Form™ ALD External Nasal Splint, Regular

    VOYAGER 6.0 SOFTWARE OPTION

    FDA 510(k)
    FDA Class 2 ·Neurology

    VITROS CHEMISTRY PRODUCTS CREA SLIDE, VIRTROS CHEMISTRY PRODUCTS CALIBRATOR KIT 1

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 23, 2025

    THREE PEG PATELLA 32MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·June 6, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 31, 2024

    12CM IQ STANDARD

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code LFL·July 24, 2024

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007

    ETS FLEX ARTICNG

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 19, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 1, 2011