BEUDAMED
    87 results · 14ms · Sources: EU EUDAMED, US FDA

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    Brand Name: Intermate Infusion Pump. Indicated for the intravenous administration of medications.

    FDA Enforcement
    Class II ·Terminated·Baxter Healthcare Corp.·July 3, 2013

    Maquet Getinge Group Operating Table System Magnus Carbon-Fibre Table Top Version 1180.16 The carbon-fibre MAGNUS table top (1180-16XX) serves to support and position patients for surgical procedures (e.g. cardiovascular surgery) and interventional examination immediately before, during and after the surgical phase. The table top is radiotranslucent and enables intraoperative use of X-ray equipment.

    FDA Enforcement
    Class II ·Terminated·Maquet Medical Systems, Usa·August 8, 2012

    SCORPIO PS TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall component fit, ligament stability, and joint range of motion prior to final implantation of the insert to the tray.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code LXH·July 13, 2010

    SCORPIO CR TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall component fit, ligament stability, and joint range of motion prior to final implantation of the insert to the tray.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code JWH·July 13, 2010

    HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy.

    FDA Enforcement
    Class II ·Terminated·Clorox Healthcare Holdings, LLC (dba HealthLink)·July 10, 2013

    SCORPIO-FLEX PS TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall component fit, ligament stability, and joint range of motion prior to final implantation of the insert to the tray.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code LXH·July 13, 2010

    SCORPIO-FLEX CR TIBIAL TRIAL, non sterile, made in the USA Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430. The Tibial trial are utilized during surgery to assess the overall component fit, ligament stability, and joint range of motion prior to final implantation of the insert to the tray.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code LXH·July 13, 2010

    Arterial Catheterization Set

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQX·July 29, 2010

    Femoral Artery Catheterization Set

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQX·July 29, 2010

    Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·July 29, 2010

    Multi-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features)

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·July 29, 2010

    Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features)

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·July 29, 2010

    Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter, ARROW g+ard Blue Catheter

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQY·July 29, 2010

    MAC Two-Lumen Central Venous Access kit with Integral Hemostasis Valve for use with 7 - 8 Fr. Catheters

    FDA Recall
    Terminated ·Arrow International Inc·Product code DYB·July 29, 2010

    Multi-Lumen Pressure Injectable Central Venous Catheterization kit with Blue FlexTip Catheter, ARROW g+ard Blue PLUS Catheter and Sharps Safety Features

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·July 29, 2010

    Two-Lumen Central Venous Catheterization kit with Blue FlexTip ARROW g+ard Blue PLUS Catheter, Sharps Safety Features, and Maximal Barrier Precautions

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·July 29, 2010

    Auto Suture ProTack Fixation 5 mm Product Catalogue # 174006. Has application in endoscopic surgery procedures.

    FDA Recall
    Terminated ·Product code GDW·February 8, 2010

    Varian Radiotherapy delivery system (C-Series Clinac, Trilogy and Novalis Tx), model numbers H14, H17, H18, H23, H26, H29, HCX

    FDA Recall
    Terminated ·Varian Medical Systems Oncology Systems·Product code IYE·June 23, 2010

    Harmony Lux Advantage LA Surgical Lighting and Visualization System, also known as the Harmony LA 700, B129382393. Designed to provide visible immunization of the surgical field or the patient and to provide audio-visual procedural support for the O.R. staff. Intended to be used in a surgical setting.

    FDA Recall
    Terminated ·Steris Corporation·Product code FTD·February 23, 2010

    Harmony Lux Classic, Surgical Lighting System, also known as the Harmony LC 500, B129388085 and B12988086. Designed to provide visible immunization of the surgical field or the patient and to provide audio-visual procedural support for the O.R. staff. Intended to be used in a surgical setting.

    FDA Recall
    Terminated ·Steris Corporation·Product code FTD·February 23, 2010