BEUDAMED
    46 results · 77ms · Sources: EU EUDAMED, US FDA

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    CMS-MST572 5F insertion kit with 5 cm tearaway. The product is shipped 10 kits per box and is intended for use in percutaneous procedures to introduce and position catheters, pacing leads and other interventional devices within the coronary and peripheral vasculature.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code DQX·April 11, 2008

    14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061423 Product Usage: An aid for introducing a hemodialysis catheter

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code LFJ·March 13, 2019

    Duo-Flow XTP Straight Full Set, RMS02105 RMS02108

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code MPB·July 12, 2018

    8F Plastic Dignity Low Profile CT Port W/Pre-Attached ChronoFlex Polyurethane Catheter

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code LJT·November 22, 2017

    Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code MSD·July 27, 2020

    Tearaway Introducer, Model # VS203, VS303, 510 K # 130687, packaged individually in a pouch, 5 pouches per carton, lot # MBZ140, MBZL450, MBZV930 MBZZ490 Product Usage: The 2F and 3F Vascu-Sheath Tearaway Introducer is intended for percutaneous venous access by modified Seldinger Technique in neonates, infants and children.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code DYB·May 5, 2016

    6.6F Plastic Dignity Low Profile CT Port W/Attachable ChronoFlex Polyurethane Catheter, Catalog # MRCTI66041, UDI#- 884908031157 Product Usage: Indicated for patient therapies requiring repeated access to the vascular system. The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples. When used with a power injectable needle, the Power Injectable Implantable Infusion Port device is indicated for power injection of contrast media.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code LJT·May 25, 2017

    12F MODIFIED Tesio CATHETER SET, REF MCTC1235SM, UDI 884908027259 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    12F X 60CM TESIO CATHETER SET WITH "Y" ADAPTOR, REF CMD757, UDI 884908005554 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    C3 Wave App, v. 2.0.5

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code LJS·October 1, 2018

    14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061425 Product Usage: An aid for introducing a hemodialysis catheter

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code LFJ·March 13, 2019

    SOFT-LINE DUO-FLOW DOUBLE LUMEN CATHETER/CATHETER SET; T94C T94M T96M T98M

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code MPB·July 12, 2018

    Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated access to the vascular system.

    FDA Recall
    Open, Classified ·Medical Components, Inc dba MedComp·Product code LJT·January 13, 2021

    CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    DUO FLOW DOUBLE LUMEN CATHETER, XTP114CT, XTP114MT, ; RAULERSON DUO FLOW IJ DOUBLE LUMEN CATHETER/CATHETER SET, XTP114IJC, XTP114IJS, XTP114IJSE, XTP114MT-C, XTP116IJC, XTP116IJS, XTP116IJSE RAULERSON PRE-CURVED DUO-FLOW IJ DOUBLE LUMEN CATHETER W/SOFT TIP SET, W/MINI SCALPEL, SYRINGE, AND NEEDLE, XTP118IJS-ID; DOUBLE LUMEN CATHETER WITH CURVED EXTENSIONS (CATHETER ONLY), XTP114IJC=, XTP116IJC=, DOUBLE LUMEN IJ CATHETER SET, XTP114IJS=, XTP115IJS=, XTP116IJS=, XTP116IJS=JO, DOUBLE LUMEN CATHETER SET, XTP114MT= DUO-FLOW DOUBLE LUMEN CATHETER, XTP116CT, INTERNAL JUGULAR CATHETER SET, XTP96IJS= (additional product codes/catalog numbers in attached spreadsheet)

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code MPB·July 12, 2018

    14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061424 Product Usage: An aid for introducing a hemodialysis catheter

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code LFJ·March 13, 2019

    Duo-Flow Double Lumen Catheter Only/Catheter Set; T114C T114M T116C T116M T116ME T118C T118M T118ME T119M

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code MPB·July 12, 2018

    12F Tesio CATHETER SET (CUFF 22CM FROM TIP), REF MCTC1235SD, UDI 884908027242 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    REPAIR KIT, REF ARA101, UDI 884908083637 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018

    REPAIR KIT, REF RPK-01, UDI 884908039856 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

    FDA Recall
    Terminated ·Medical Components, Inc dba MedComp·Product code NFK·February 23, 2018