BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    EAGLE 3000/3100 PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LOCOBASE WOUND AND SKIN EMULSION

    FDA 510(k)
    FDA Unclassified ·Unknown

    Endophys Pressure Sensing Sheath Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TITANIUM NEXGEN LCCL FEMORAL SZ C-LT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 21, 2018

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 14, 2013

    FOUNDATION SHOULDER

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code KWS·January 7, 2011

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 28, 2014

    NEXGEN LEGACY POSTERIOR STABILIZED ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 16, 2016

    ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026