BEUDAMED
    13 results · 28ms · 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 ×

    ESPOCAN COMBINED SPINAL/EPIDURAL NEEDLE SET & TRAY

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10885380083426·3.2mm Guide Wire 400mm

    GALAXY FIXATION SYSTEM

    FDA UDI
    ORTHOFIX SRL·18033509859311·ROD D 12 MM L 400 MM

    ASNIS

    FDA UDI
    Stryker GmbH·04546540534354·Tray

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102886·BECHERT NUCLEUS ROTATOR 7MM

    Galaxy Fixation System

    FDA UDI
    ORTHOFIX SRL·18033509859649·ROD D 12 MM L 400 MM STERILE

    LAFACI

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

    LP(A) CALIBRATORS, AND LP(A) CONTROLS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ASPHERE M SPEC 12/14 40 +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 17, 2014

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 17, 2014

    CARE ASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FNL·January 7, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·December 17, 2010

    PFC*SIGMA/RD/DOME PAT 3PEG,35

    FDA Adverse Event
    Injury ·DEPUY IRELAND ¿ REG. # 9616671·Product code JWH·July 14, 2014