BEUDAMED
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    FINE SURGICAL CIRCUMCISION CLAMP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Direct Supply

    FDA UDI
    Hoffmann NOA Medical Industries, LLC·00817492013155·TRAPEZE - Floor - Direct Supply Bariatric (Beige)

    ODYSSEY®

    FDA UDI
    Microport Orthopedics Inc.·M684K00400521·

    NA

    FDA UDI
    Stryker GmbH·00886385009124·End Cap, Right A3 Nail 10mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410400520·Anterior Closing Wedge Osteotomy Guide, 40mm x ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420400520·Anterio Lateral Closing Wedge Osteotomy Guide, ...

    NA

    FDA UDI
    ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024311060·

    Processor, Cervical Cytology Slide, Automated

    FDA Pre-Market Approval
    FDA Class 3 ·MONOPREP PAP TEST

    X-RAY MONOBLOCK, MONOBLOCK XRS-60-330

    FDA 510(k)
    FDA Class 1 ·Radiology

    RESPIRONICS BILICHEK NON-INVASIVE-100-0800-20; BILIRUBIN ANALYZER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Processor, Cervical Cytology Slide, Automated

    FDA Pre-Market Approval
    FDA Class 3 ·MONOPREP PAP TEST

    Processor, Cervical Cytology Slide, Automated

    FDA Pre-Market Approval
    FDA Class 3 ·MONOPREP PAP TEST

    Processor, Cervical Cytology Slide, Automated

    FDA Pre-Market Approval
    FDA Class 3 ·MONOPREP PAP TEST

    Processor, Cervical Cytology Slide, Automated

    FDA Pre-Market Approval
    FDA Class 3 ·MONOPREP PAP TEST

    Processor, Cervical Cytology Slide, Automated

    FDA Pre-Market Approval
    FDA Class 3 ·MONOPREP PAP TEST

    Processor, Cervical Cytology Slide, Automated

    FDA Pre-Market Approval
    FDA Class 3 ·MONOPREP PAP TEST

    Processor, Cervical Cytology Slide, Automated

    FDA Pre-Market Approval
    FDA Class 3 ·MONOPREP PAP TEST

    HIRES 90K IMPLANT

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·April 3, 2013

    INFERIOR PLATE LARGE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MJO·May 8, 2008

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 5, 2011