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

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    Filters Regulation: Us FDA ×

    SP-1000, SP-2000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113394·MICS TRAP KNIFE 1.8/2.2 (BX/5)

    Accufit

    FDA UDI
    Ortho Organizers, Inc.·00190707184193·Accufit Molar Bands Lower Left Second Molar 39 1/2

    MODEL 30 CLASSIC PNEUMATONOMETER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    1.5T SCANMED PV ARRAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·January 10, 2024

    BD ULTRA-FINE¿ PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·June 2, 2023

    AVON PAT/FEM JOINT EX SMALL

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code KRR·August 4, 2011

    HUDSON ET TUBE, UNCUFFED, PED-SOFT, 2.5MM

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BTR·September 15, 2014

    UNKNOWN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 25, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 25, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 25, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 25, 2022

    VENA SEAL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code PJQ·December 21, 2023

    EVERFLEX+ SELF-EXPANDING PERIPHERAL STENT SYSTEM STANDARD

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIP·November 17, 2023

    VISI-PRO BALLOON-EXPANDABLE STENT SYSTEM

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIO·November 17, 2023

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 25, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 25, 2022