BEUDAMED
    10 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 ×

    Protek Solo 24 Fr Venous Cannula Set

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550131·GENUMEDI PT KNEE SUP SILVER L EW IV

    REACH(R) FEMORAL PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304307025·

    CRYOPEN CRYOSURGICAL SYSTEM, K102214

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

    BRACHYSCIENCES STRANDPORT

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENDO FLIP

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    UNKNOWN TRIDENT CERAMIC ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·July 7, 2011

    SIMPLEX P - US TOBRA FD 10-PK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LOD·June 11, 2013

    NEXGEN COMPLETE KNEE SOLUTION CRUCIATE RETAINING (CR) PROVISIONAL-ARTICULAR SURF

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·September 3, 2008

    TRUE METRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·February 1, 2022