BEUDAMED
    9 results · 25ms · 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.

    DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SeaSpine Spacer System - Hollywood™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981058425·18mm Hollywood Trial, Lordotic

    SeaSpine Spacer System - Hollywood™

    FDA UDI
    Seaspine Orthopedics Corporation·10889910058427·18mm Hollywood Trial, Lordotic

    JAKOBI SURG. INSTRUMENTS #7 10/43

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    CIBA CORNING MODEL 238 PH/ BLOOD GAS ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    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

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·January 30, 2013

    AXIOM SIRESKOP SD

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code MQB·December 17, 2010

    SPECTRUM INFUSION PUMP

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