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

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    SMITH & NEPHEW CANNULATED SCREWS AND WASHERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101

    FDA 510(k)
    FDA Unclassified ·Unknown

    APEX KNEE MODULAR TIBIA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·October 19, 2005

    CD SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK EUROPE·Product code KWQ·April 19, 2000

    TSRH SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code KWP·May 19, 1999

    SALEM SUMP TUBE

    FDA Adverse Event
    Malfunction ·SHERWOOD DAVIS AND GECK·Product code KNT·March 12, 1997

    MEDCHEM PRODUCTS

    FDA Adverse Event
    Injury ·MEDCHEM PRODUCTS, INC.·Product code FGH·February 9, 1995

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·February 26, 1999

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·February 20, 2013

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - CORK·Product code KNQ·September 7, 2012

    *

    FDA Adverse Event
    Malfunction ·*·Product code DQO·March 9, 1998

    CRE? WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·June 18, 2013

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·January 7, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 7, 2013

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 2, 2011

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·March 13, 2013

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·August 10, 2012

    AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·May 28, 2014