BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CASCADIA™ Interbody System

    FDA UDI
    VB Spine LLC·10888857554634·Trial Size 14x18x14 mm, Convex

    Identity Imprint Porous CR

    FDA UDI
    Conformis, Inc.·M572POV0123809011·POROUS OVAL PATELLA, 38MM X 9MM, iPoly

    HITACHI CLINICAL ANALYZER S TEST REGENT CARTRIDGE C-REACTIVE PROTEIN (CRP)

    FDA 510(k)
    FDA Class 2 ·Immunology

    Advin Multi-Drug Screen Test Cassette, Dip Card and Cup

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    AMISTEM H FEMORAL STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code LZO·April 26, 2013

    UNKNOWN HIP HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code KWY·May 22, 2013

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DSI·June 14, 2011

    LEAD MODEL UNKNOWN

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 15, 2008

    INSTINCT ENDOSCOPIC HEMOCLIP

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code PKL·July 19, 2021

    INSTINCT ENDOSCOPIC HEMOCLIP

    FDA Adverse Event
    Injury ·WILSON-COOK MEDICAL INC·Product code PKL·September 12, 2022