BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Electronic Sphygmomanometers

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Caplugs/Evergreen

    FDA UDI
    CAPlugs·00810044204780·TEST TUBE 17X100MM 2-POS CAP

    RUBICON 18 SUPPORT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EZMANAGER PLUS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IMP,TSV,6.0,10,MTX,MG

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·October 7, 2021

    AC POWER MODULE

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·July 15, 2011

    SIG FEM ADPT TORQUE WRENCH

    FDA Adverse Event
    Malfunction ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LXH·November 4, 2014

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·July 12, 2013

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

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