BEUDAMED
    37 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF MONODERM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    QUILL SRS

    FDA Adverse Event
    Malfunction ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·September 3, 2008

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·February 13, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP (DBA ANGIOTECH)·Product code NEW·March 15, 2010

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

    QUILL KNOTLESS TISSUE-CLOSURE DEVICE

    FDA Adverse Event
    Injury ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·May 11, 2011

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·July 26, 2012

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 19, 2010

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·January 5, 2011

    QUILL KNOTLESS TISSUE CLOSURE DEVICE

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·October 31, 2011

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·July 10, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·July 15, 2009

    QUILL KNOTLESS TISSUE CLOSURE DEVICE

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·October 26, 2011

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP.·Product code NEW·November 8, 2013

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·September 22, 2010

    Vial Adapter

    FDA UDI
    WEST PHARMA. SERVICES IL, . LTD·07290108240009·Vial Adapter 20mm ML TG SS Blue SIL- VF

    Optimus Drill Q - 3.5mm 55mm

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215061678·

    ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-5

    FDA 510(k)
    FDA Unclassified ·Unknown

    BRAVO PH MONITORING SYSTEM

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology