BEUDAMED
    22 results · 23ms · 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 ×

    DIGITAL BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SBRT Secure Arch, size S

    FDA UDI
    MACROMEDICS B.V.·08719425702599·SBRT Secure Arch, size S

    FOERSTER SPONGE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896021556·FOERSTER SPONGE FORCEPS STRAIGHT SMOOTH JAW

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K1230000·Rod Holder, Curved, 5.5 mm

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702271300·Elvarex 3/Thigh High/Slant, Closed Toe, Knee Co...

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011123600000·Hard metal burs, drilltoothed, straight, Form: ...

    IMMUNOCAP RAPID READER, MODEL 12-3600-10

    FDA 510(k)
    FDA Class 2 ·Immunology

    BD INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·April 17, 2025

    PUENTE TORNADO

    FDA UDI
    The Wells Johnson Company·B458201236000·Cannula, Puente Tornado, specify length, diamet...

    PORTABLE X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    IM BAND

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    BD INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·April 24, 2025

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 31, 2023

    BD INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 14, 2025

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 17, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 26, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·June 14, 2011

    LIFEPAK® 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019

    BD INSYTE AUTOGUARD YEL 24GA X .75IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·February 6, 2025