BEUDAMED
    27 results · 23ms · Sources: EU EUDAMED, US FDA

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    BONART ART-M3II & M4 ULTRASONIC SCALER UNITS WITH ACCESSORIES (INSERTS)

    FDA 510(k)
    FDA Class 2 ·Dental

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809847826·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE LARGE-LO...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710400520280·Anterior Dome Osteotomy Guide, 52mm x 28mm

    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

    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

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code JDI·April 11, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 2, 2014

    MICRO-AIRE DRILL BIT

    FDA Adverse Event
    MICROAIRE SURGICAL INSTRUMENTS, LLC·Product code HTW·May 15, 2008

    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

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    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

    CryoValve SG Cryopreserved Pulmonary Human Heart Valve

    FDA Enforcement
    Class II ·Ongoing·Artivion, Inc·April 24, 2024