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

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    Patient Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113363·CLEAR CORNEA KNIFE 3.0MM (BX/5)

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113417·IMPLANT KNIFE 5.2MM (BX/5)

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113349·PHACO KNIFE 3.2MM ANGLED (BX/5)

    MS104A, NEWMINI II (EMS-II), MODEL AP-101050T AND MEDTRIM (EMS-V), MODEL AP-102050T

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BALDUR BRAND VINYL POWDERED EXAMINATION GLOVES, SUN FLOWER GLOVES CO., LTD

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    FASTRAC GASTRIC ACCESS PORT SAFETY SYSTEM

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS, INC.·Product code KNT·October 15, 2008

    URETEX SUPPORT PP KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·June 21, 2013

    HIRES 90K

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·August 8, 2011

    UNKNOWN LIGASURE INSTRUMENT

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·July 24, 2024

    VALIANT CAPTIVIA UNK

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·May 15, 2024

    VALIANT NAVION

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·May 15, 2024

    VALIANT CAPTIVIA UNK

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·May 15, 2024

    VALIANT NAVION

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·May 15, 2024

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

    FDA Adverse Event
    Death ·HEARTWARE, INC.·Product code DSQ·December 13, 2023

    VCL+ UD 18IN 5-0 S/A PS-3 PRM MP

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·February 15, 2023

    UNK LINX MAGNETIC IMPLANT

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·April 11, 2024

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·May 6, 2024

    GROSHONG 4F SL PICC PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER BASIC

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code DQY·September 18, 2023