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

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    VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LYNX

    FDA UDI
    HNM TOTAL RECON LLC·00841742110745·LYNX ø3.5mm Std Cortical Screw, Full Thread, Se...

    RESPONDER 3000

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    NEUROPLUS, MODEL A10040, A10041, A10042, A10043

    FDA 510(k)
    FDA Class 2 ·Neurology

    CONTOUR CURVED CUTTER STAPLER CS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 13, 2006

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·March 23, 2022

    CADD MEDICATION CASSETTE

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·July 14, 2022

    CADD

    FDA Adverse Event
    Malfunction ·NULL·Product code FPA·August 17, 2021

    CADD MEDICATION CASSETTES

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2022

    PFC*SIGMA/OV DOME PAT 3 PEG,32

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code JWH·April 8, 2013

    ENDEAVOR ZOTAROLIMUS-ELUTING CORONARY STENT OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·May 8, 2008

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·April 6, 2011

    The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018