BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    CARDIAC INSULATION PAD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BR2000 BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919100720·K7-1990-50

    Brasseler

    FDA UDI
    Provision·B504OMK71990500·

    NA

    FDA UDI
    STERILMED, INC.·10888551016148·SAW BLADE OSCILLATING AGGRESSIVE CUT LARGE BONE

    LUBRICANO STERILE GEL

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OMNIMEDICAL 400L

    FDA 510(k)
    FDA Class 2 ·Radiology

    PK DISSECTING FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 30, 2014

    HOVERMATT LATERAL PATIENT TRANSFER DEVICE

    FDA Adverse Event
    Injury ·D.T. DAVIS ENTERPRISES LTD. T/A HOVERTECH INTERNATIONAL·Product code FRZ·September 18, 2012

    LIGACLIP MCA SMALL APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDO·January 30, 2008

    K7-1990-50 90.0 X 19.0 MM 1.27+

    FDA Adverse Event
    Malfunction ·BRASSELER USA·Product code GFA·April 14, 2023

    Comprehensive HHR Tess Cleat, Item Nos. 110260 110261 110262 110263 Product Usage: N/A

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019