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

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    FDI LEVEL I AND LEVEL II GLUCOSE CONTROLS FOR THE EMBRACE NO CODE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Oticon

    FDA UDI
    Oticon A/S·05707131260963·RIA, MINIRITE 312 WL TC

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613070779·Metzenbaum (Lahey) Scissors, Super Cut, Straigh...

    INOGEN SATELLITE CONSERVER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    APC FLASH-FREE ADHESIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    M.U.S.T. PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

    PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

    MULTILOC HN Ø8.5 LE CANN L270 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HSB·May 29, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·May 4, 2011

    REACH CLEANSEPASTE TARTAR CONTROL FLOSS

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON HEALTHCARE PRODUCTS·Product code JES·August 21, 2008

    MECTALIF POSTERIOR

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 2025

    MECTALIF OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12X28X7 L0°

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·November 10, 2017

    BD PHASEAL PROTECTOR P50J

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·July 7, 2023

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·May 17, 2019

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·March 18, 2019

    OPTILITE SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·June 5, 2020

    MECTALIF (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI 11X22X7 L5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 29, 2020

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 LONG HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 23, 2019

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·May 25, 2023

    COOK® SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·March 12, 2019