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

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    Hospira Extension Set, Hospira Primary Set

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304250970·

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707066286·KOBAYASHI PREFORMED WIRE 014"

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613098896·Freeman Face Lift Rake Retractor, 4 Prongs, Sma...

    SHIMADZU COLLIMATOR R-20J

    FDA 510(k)
    FDA Class 2 ·Radiology

    EASYRA HDL REAGENT; EASYRA LDL REAGENT; EASYRA CHOL REAGENT; EASYRA TRIG REAGENT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·February 21, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 13, 2011

    OT VERIO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWP·October 10, 2014

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 25, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 25, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 26, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·December 31, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·December 31, 2019

    COMPRESS SEGMENTAL FEMORAL REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 13, 2017

    ORTHOPEDIC SALVAGE SYSTEM- OSS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KRO·July 13, 2017

    COMPRESS ANTI-ROTATION SPINDLES

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 13, 2017

    COMPRESS SEGMENTAL FEMORAL REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 13, 2017

    COMPRESS SEGMENTAL FEMORAL REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 13, 2017