BEUDAMED
    21 results · 52ms · Sources: EU EUDAMED, US FDA

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    UNK

    FDA Adverse Event
    Injury ·CIRCON OHIO OFFICE·Product code GEH·March 24, 1998

    FALOPE RING BAND

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code HFY·February 24, 1994

    PLEATMAN SAC INTRODUCER

    FDA Adverse Event
    Injury ·CABOT MEDICAL CORP.·Product code HET·February 24, 1994

    LAPAROSCOPIC GRASPER

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code GEN·March 14, 1995

    FALOPE RING BAND

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code HFY·November 17, 1994

    KLI MEDICAL

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code KNH·June 11, 1997

    *

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code GCJ·April 1, 1997

    CHOLANGIOGRAPHY INSTRUMENT

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code GCJ·October 21, 1996

    SYSTEM 2001 ELECTRONIC INSUFFLATOR

    FDA Adverse Event
    Injury ·CABOT MEDICAL CORP.·Product code HIF·November 26, 1996

    CRYOMEDICS 110-G ELECTROSURGICAL UNIT

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code GEI·October 4, 1996

    CRYOTIP

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code GEH·January 21, 1997

    TUBAL OCCLUSION BAND

    FDA Adverse Event
    CABOT MEDICAL CORP·Product code HFY·January 29, 1997

    KCI FALLOPE RING BAND

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code HFY·August 22, 1994

    BERKLEY VACUUM CURETTAGE SYSTEM

    FDA Adverse Event
    Injury ·CABOT MEDICAL CORP.·Product code HGG·November 23, 1999

    PLEATMAN SAC TISSUE RETRIEVAL DEVICE

    FDA Adverse Event
    Injury ·CABOT MEDICAL CORP.·Product code GCJ·September 18, 1995

    BANDING INSTRUMENT

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code KNH·January 29, 1996

    FALOPE-RING BAND

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP.·Product code KNH·January 12, 1996

    BERKLEY VC-5

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL CORP·Product code JCX·October 26, 2002

    FALOPE-RING TUBAL OCCLUSION BAND

    FDA Adverse Event
    Malfunction ·CABOT MEDICAL PRODUCTS CORP.·Product code HFY·December 28, 1995

    SURGITEK MAMMARY IMPLANTS

    FDA Adverse Event
    SURGITEK DIV OF CABOT MEDICAL ENGINEERING CORP·Product code FTR·July 2, 1996