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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    INTRAN 500

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Nexxis OR

    FDA UDI
    Barco NV·05415334042346·NEXXIS WORKSPOT KIT2 CM

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295238096·P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ ...

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471149816·K-WIRE - DOUBLE TROCAR FULLY THREADED 1.2mm DIA...

    Phasix Mesh

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

    CELSITE/ CELSITE CONCEPT, ACCESS PORTS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENDO STITCH 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·May 29, 2014

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 18, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 14, 2011