BEUDAMED
    12 results · 22ms · 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 ×

    CARDIOLIPIN AUTOANTIBODY IMMUNOLOGICAL TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16740918450·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674091845060·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450311820·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587C09184540·9mm H x 18mm W x 45mm L x 4 degree XLIF Coronal...

    WAVEWRITER ALPHA PRIME 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 23, 2023

    MALLINCKRODT, GOODKNIGHT 418S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MILLCOMP

    FDA 510(k)
    FDA Class 2 ·Radiology

    CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 17, 2011

    PASSPORT 2 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code DSI·April 30, 2013

    THIN-WALLED FEP RINGED GORE-TEX STRETCH VASCULAR GRAFT WITH REMOVABLE RINGS (LIN

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·July 31, 2008

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 14, 2019