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

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    Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Ophthalmic Spatulas

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114322·RUBENSTEIN CORNEAL ROLLER (BX/3)

    MALLINCKRODT, GOODKNIGHT 418S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    STARDUST II, MODEL 1011176

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Widex

    FDA UDI
    Widex A/S·05706069773736·Widex EVOKE E-FS (Shocking pink S-440 ) Telecoi...

    WATCHMAN FLX LEFT ATRIAL APPENDAGE CLOSURE DEVICE WITH DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·July 31, 2019

    HOMECHOICE AUTOMATED PD SET W/CASSETTE 8-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 21, 2008

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011

    Y-KNOT ALL-SUTURE ANCHOR WITH 1 #2 BLUE/WHITE HIFI SUTURE

    FDA Adverse Event
    Injury ·CONMED LINVATEC·Product code MBI·July 2, 2013

    BD PEGASUS SAFETY CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·July 8, 2020

    SPINNING SPIROS CLOSED MALE LUER, RED CAP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·November 1, 2018

    MEDTRONIC NAVIGATION

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC·Product code HAW·December 8, 2020

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·November 11, 2020

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·December 26, 2018

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·December 26, 2018

    UNK - PLATES: FOOT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code JEY·September 9, 2022

    UNK - GUIDE/COMPRESSION/K-WIRES

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code LRN·September 9, 2022

    UNK - SCREWS: 3.5 MM CORTEX

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·September 9, 2022

    SELECTSECURE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVN·March 28, 2018

    FMC BLOODLINE

    FDA Adverse Event
    Injury ·ERIKA DE REYNOSA, S.A. DE C.V.·Product code FJK·December 17, 2018