BEUDAMED
    81 results · 22ms · 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 ×

    SURGEON'S GLOVE, POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Armada

    FDA UDI
    Nuvasive, Inc.·00887517208255·ARM15T Rod, 30mm Conventional Pre-Bent

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809847840·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE LARGE FU...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197532822·Vascular Metzenbaum Scissors Ø5mm, ...

    Implant-One

    FDA UDI
    Implant Logistics, Inc.·D762APT0520300·Abutment, 500 Series Angled Post 2mm Cuff Heigh...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710400520300·Anterior Dome Osteotomy Guide, 52mm 30mm

    PORTABLE INTENSIVE CARE UNIT

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    .020" NITINOL GUIDEWIRE

    FDA Adverse Event
    Other ·DATASCOPE CORP.·Product code DQX·September 27, 1999

    .020" NITINOL GUIDEWIRE

    FDA Adverse Event
    Other ·DATASCOPE CORP.·Product code DQX·September 24, 1999

    .020" NITINOL GUIDEWIRE

    FDA Adverse Event
    Other ·DATASCOPE CORP.·Product code DQX·September 24, 1999

    .020" NITINOL GUIDEWIRE

    FDA Adverse Event
    Other ·DATASCOPE CORP.·Product code DQX·September 24, 1999

    .020" NITINOL GUIDEWIRE

    FDA Adverse Event
    Other ·DATASCOPE CORP.·Product code DQX·September 27, 1999

    ARCHITECT CA19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·October 31, 2025

    HYPODERMIC NEEDLE-PRO EDGE SAFET

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC. / ICU MEDICAL, INC.·Product code FMI·November 7, 2025

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 19, 2026

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 4, 2013

    AUTOCAT2 WAVE

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·March 2, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 21, 2008

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 1, 2026