BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    NON-CONTACT CLINICAL THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TASMIN R 12°

    FDA UDI
    SIGNUS Medizintechnik GmbH·04047844014905·The basic shape of the TASMIN R devices is a ho...

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 27, 2020

    MaxFuse VBR, 10 (D) x 12 (W) x 47 (H)

    FDA UDI
    Pioneer Surgical Technology, Inc.·00846468055486·10 (D) x 12 (W) x 47 (H)

    CLINITEK ATLAS PRO 12 REAGENT PAK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OTSC (OVER-THE SCOPE-CLIP) SYSTEM SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 19, 2025

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929059524·Convexx Corpectomy, 12Dx14Wx28H, 6°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929034347·Corpectomy, 12Dx14Wx28H 6°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929034156·Corpectomy, 12Dx14Wx28H 0°

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 6, 2011