BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    ATI DISPOSABLE TEST PACK FOR EO GAS STERILIZATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295230526·P.F.C. SIGMA TIBIAL INSERT ROTATING PLATFORM RP...

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482149294·Symmetry® Forceps; Dissector; Right Angled; Non...

    POLYAXIAL HEMISPHERICAL SPINAL SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Monitor B40

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM, DEXCOM SHARE SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 29, 2015

    V200 VENTIALTOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·July 22, 2014

    CONTAK RENEWAL

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 6, 2011

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022