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

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    SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Channel Drain

    FDA UDI
    C. R. Bard, Inc.·00801741119163·Novaplus Channel Drain, 15Fr. Round Hubless Ful...

    Channel Drain

    FDA UDI
    C. R. Bard, Inc.·00801741049880·Channel Drain, 15Fr. Round Hubless Full Fluted

    FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES

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

    PHOTON MODULAR WORKSTATION SYSTEM, MODELS Z-12834-X & Z-13175-X

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

    AVISTA MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 30, 2021

    SYRINGE 0.3ML 30GA 1/2IN UF 500CS

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·May 8, 2020

    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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·April 28, 2011

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·July 10, 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

    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