BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    COHORT BONE BRUSH

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123021·K-WIRE - SINGLE TROCAR 2.0mm DIA x 200mm

    ID-RING

    FDA UDI
    DiaDent Group International·08806383525619·Used for color coding files

    RT ELEMENTS, DOSE REVIEW, BRAIN METASTASES, ADAPTIVE HYBRID SURGERY ANALYSIS

    FDA 510(k)
    FDA Class 2 ·Radiology

    VISTA PLUS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SUMMIT POR TAPER SZ6 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 4, 2013

    TERUMO VIRTUOSAPH VEIN HAVESTING SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·November 11, 2010

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 17, 2014

    Philips Zenition 70, Model Number: 718133

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024