BEUDAMED
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    CHAD THERAPEUTICS BONSAI MODEL 800

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Closed Wound Suction

    FDA UDI
    C. R. Bard, Inc.·00801741049569·100cc Silicone Closed Wound Suction Evacuator w...

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496070740·SECRET SKIN, SIZE XXL, NERO, MICRO-MASSAGING PO...

    ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FG-36UX, FIBER ULTRASOUND GASTROSCOPE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PVC DRAIN WITH TROCAR

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GBX·August 23, 2022

    WOUND DRAINAGE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GCY·September 14, 2022

    PVC DRAIN WITH TROCAR

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GCY·August 25, 2022

    PVC DRAIN WITH TROCAR

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GBX·August 23, 2022

    BLAKE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GBX·June 10, 2025

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 30, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

    BARD WOUND DRAIN

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GBX·August 23, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

    SILICONE ROUND DRAIN

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code GBX·July 30, 2025

    BARD 100CC SILICONE BULB EVACUATOR 0070740

    FDA Adverse Event
    Injury ·BARD MEDICAL·Product code GCY·December 28, 2010

    CHANNEL DRAIN

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code GBX·December 11, 2024

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 22, 2013

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 14, 2011

    PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC.·Product code DQY·July 1, 2008