BEUDAMED
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    COBE BRAT 2 AUTOLOGOUS BLOOD SALVAGE SYSTEM WITH THE CRIT-LINE HEMATOCRIT SAMPLING SYSTEM OPTION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DESS Dental Smart Solutions

    FDA 510(k)
    FDA Class 2 ·Dental

    FIX. & LENS FOR. #'S 3510,3512,3248,3795

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    11G BLADED MAMMOTOME ST PROBE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code KNW·February 27, 2006

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 7, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·August 8, 2014

    LUMAX 340 DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK, SE & CO. KG·Product code MRM·February 7, 2011

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 30, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·November 24, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 15, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 9, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 4, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 24, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·January 12, 2026

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·March 4, 2026

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·February 19, 2026