BEUDAMED
    12 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    Medos International Sàrl·10886705032143·HD C-Mount Arthroscope/Sinuscope compatible wit...

    Artman Instruments

    FDA UDI
    Wise Linkers, LLC·D1272422761·Dental Mirrors Set of 5 Cone Socket Blue Plasm...

    MORELAND

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295123453·MORELAND REV INST MEDIAL OSTEOTOME 15mm

    D-VAPOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MCS Bone Graft

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERSATAP SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·ORTHO-DESIGN·Product code MBI·September 15, 2025

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 4, 2015

    EQUINOXE, HUMERAL STEM PRIMARY, PRESS FIT 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code HSD·July 12, 2024

    GDC-10 SOFT 2D SR COIL

    FDA Adverse Event
    Injury ·NEUROVASCLAR DIVISION, BOSTON SCIENTIFIC CORP·Product code HCG·November 19, 2008

    UNICEL DXL800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 10, 2011

    SUMMIT POR TAPER SZ7 STD OFF

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code MRA·July 23, 2013