BEUDAMED
    26 results · 24ms · Sources: EU EUDAMED, US FDA

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    NCompass Nitinol Stone Extractors

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

    N-COMPASS NITINOL STONE EXTRACTOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·April 1, 2022

    N-COMPASS NITINOL STONE EXTRACTOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·April 1, 2022

    N-COMPASS NITINOL STONE EXTRACTOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·April 1, 2022

    N-COMPASS NITINOL STONE EXTRACTOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·August 25, 2022

    N-COMPASS NITINOL STONE EXTRACTOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·February 3, 2021

    N-COMPASS NITINOL STONE EXTRACTOR

    FDA Adverse Event
    Injury ·COOK INC·Product code LQR·January 8, 2025

    N-COMPASS NITINOL STONE EXTRACTOR

    FDA Adverse Event
    Injury ·COOK INC·Product code LQR·February 10, 2022

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707001454·MEMORIA SPRINGS FIRST CLASS .

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 26, 2022

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 26, 2022

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 26, 2022

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 26, 2022

    SENTICARE PILLSTATION

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ONEPORT SURGICAL TROCAR SYSTEM

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

    CLOVERLEAF FUSION PL 2.4/2.7 VA LOCK 2HO

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·June 17, 2013

    FLEXTEND II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 23, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008

    Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model Number (REF): 782105. 510(k) Numbers: K173079, K183063, K193215, K213583, K223458, K251397, K251808.

    FDA Recall
    Open, Classified ·Philips North America·Product code LNH·April 14, 2026

    Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model Number (REF): 782103. 510(k) Numbers: K163116, K173079, K183063, K193215, K213516, K213583, K223458, K251397, K251808

    FDA Recall
    Open, Classified ·Philips North America·Product code LNH·April 14, 2026