BEUDAMED
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    DMR/CO2 COMBO KTI

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KTI TRANSPARENT WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    KELLER-TIMMERMANS STRAIGHT GUIDING SHEATH

    FDA Adverse Event
    Injury ·COOK INC.·Product code DYB·April 24, 2009

    KTI HY-Q(TM) WOUND DRESSING

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LA DIFFUSION TECHNIQUE, KTY CM-10 BREAST PUMP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ENDOPATH DISPOSABLE SURGICAL TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. S.A. DE C.V.·Product code GCJ·January 8, 1999

    ACCURUS 800CS

    FDA Adverse Event
    Injury ·ALCON - HOUSTON·Product code HQE·February 20, 2004

    CRE¿ PULMONARY

    FDA Adverse Event
    Malfunction ·Product code KTI·October 26, 2017

    GORE TAG THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·W.L. GORE & ASSOCIATES·Product code MIH·September 25, 2009

    ENDOPATH TRISTAR BLUNT TIP SURGICAL TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. S.A. DE C.V.·Product code GCJ·February 12, 1999

    KTI SPECIAL SET

    FDA Adverse Event
    Injury ·COOK INC.·Product code KTI·October 9, 2007

    CRE¿ PULMONARY

    FDA Adverse Event
    Malfunction ·Product code KTI·July 30, 2018

    CRE¿ PULMONARY

    FDA Adverse Event
    Malfunction ·Product code KTI·January 30, 2018

    CRE¿ PULMONARY

    FDA Adverse Event
    Malfunction ·Product code KTI·April 26, 2018

    CSF DRAINAGE KIT CONSISTS OF 10-110/10-450

    FDA Adverse Event
    Death ·CLINICAL NEURO SYSTEMS·Product code JXG·December 11, 2003

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·September 8, 2014

    HEMODIALYSIS TWO-LUMEN KTI: 2-

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code MSD·March 22, 2007

    MAJ-210 (20PCS)

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·July 6, 2016

    MAH ELITE KTI 13.5FR 16CM CE

    FDA Adverse Event
    Other ·COSTA RICA COVIDIEN MANUFACTURING·Product code MSD·July 14, 2014

    TELIX K TI CAGE, 9X28MM 5°

    FDA Adverse Event
    Injury ·BIEDERMANN MOTECH GMBH & CO. KG·Product code MAX·April 5, 2018