BEUDAMED
    10 results · 34ms · Sources: EU EUDAMED, US FDA

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    FINE NEEDLE ASPIRATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOPHYS PRESSURE SENSING SHEATH KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROCERA ABUTMENT OCTAGON

    FDA 510(k)
    FDA Class 2 ·Dental

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·May 30, 2014

    PARIETEX UGYTEX PP POSTERIOR KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·October 25, 2012

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INTRAOCUL

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·September 15, 2010

    ANATOMICAL SHOULDER¿¢ DOMELOCK®, DOME, CENTRIC

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 21, 2023

    ANATOMICAL SHOULDER¿¢, HUMERAL STEM, UNCEMENTED, ø 10.5, 100 MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 20, 2023

    ANATOMICAL SHOULDER¿¢ DOMELOCK®, HUMERAL HEAD, ø 44-16, R=24.4MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 20, 2023

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015