BEUDAMED
    11 results · 29ms · Sources: EU EUDAMED, US FDA

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    PHOSPHOLIPID REAGENT SET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    EZ

    FDA UDI
    CENTRIX, INC.·00817051022871·Syringe AY III EZ BLUE

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112298·SURG-I-BAND BLACK

    Solstice Occipito-Cervico-Thoracic System

    FDA UDI
    Life Spine, Inc.·00190837040857·Solstice Smooth Shaft Assembly, 4.0 x 40mm long

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0140400·Driver Shaft, T30 Final Cap Driver

    ClearPoint Array System (version 1.1)

    FDA 510(k)
    FDA Class 2 ·Neurology

    FAMILY OF ALTUS MEDICAL MODIFIED COOLGLIDE AESTHETIC LASERS, MODELS COOLGLIDE I, II AND FUTURE MODELS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LGC TIBIAL FIT TRAY CEM SZ 5F / 4T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 23, 2024

    MBT CEM KEEL TIB TRAY SZ3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·December 1, 2010

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·January 14, 2013

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·HEARTWARE, INC·Product code DSQ·July 3, 2014