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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Arm Blood Pressure Monitor, models AOJ-30A, AOJ-30B, AOJ-30C, AOJ-30D, AOJ-30E, AOJ-30F and AOJ-30G

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    WELMED INC.·00849296000727·

    Tissue Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112847·BARRON ARTIFICIAL ANTERIOR CHAMBER

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707100607·EXACONNECT PLUS 2.2 ANG.25°GH1,5

    DIALYZER

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code FJI·May 2, 1996

    ASA LASER SH1

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PROVOX FREEHANDS HME, MODEL 7710

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 13, 2025

    FREESTYLE LIBRE 3 PLUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code QBJ·May 19, 2026

    THERMACHOICE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code MKN·November 5, 2008

    GALILEO ECHO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·August 24, 2011

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 2, 2013