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

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    MAMMOMAT Revelation

    FDA 510(k)
    FDA Class 2 ·Radiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471129450·K-WIRE - DOUBLE TROCAR WITH GUIDE 1.6mm DIA x 1...

    WITTMANN PATCH

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

    CHEETAH RELIANT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEARTSMART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LDD·October 7, 2008

    ECHELON*FLEX60 LONG

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 27, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 22, 2011

    Allura Xper FD10; Model Numbers: (1) 722003, (2) 722010, (3) 722026; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 8, 2025