BEUDAMED
    11 results · 18ms · 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.

    COAGULATION REFERENCE PLASMA, NORMAL

    FDA 510(k)
    FDA Class 2 ·Hematology

    WaveForm TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981243746·Interbody, 9mm x 32mm x 14mm, 15 Deg, 3D

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981202576·Interbody, 9mm x 32mm x 14mm, 15 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981194581·Interbody, 9mm x 32mm x 14mm, 15 deg

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150577·K-WIRE - DOUBLE TROCAR 1.4mm DIA x 125mm

    AUDICOR UPGRADE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MTM(R) CLEAR ALIGNER

    FDA 510(k)
    FDA Class 2 ·Dental

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 25, 2013

    OPEN SPINE CLAMP, TITANIUM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·December 14, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014