BEUDAMED
    182 results · 28ms · Sources: EU EUDAMED, US FDA

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    TELEFLEX LLC Arrow Central Venous Catheter Kit 16, 18 Gauge Multi Lumen Model Number:CDC-45703-XP1A (Model Numbers # IPN035619, IPN036437, IPN922677)

    FDA Recall
    Open, Classified ·Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233·Product code FOZ·May 25, 2022

    Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or tissue ligation

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code FZP·April 28, 2023

    Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic dialysis grafts.

    FDA Recall
    Terminated ·TELEFLEX MEDICAL INC·Product code QEW·January 11, 2022

    Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), PT-45509 containing components: PT-45509-S6, PT-45509-T The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic dialysis grafts.

    FDA Recall
    Terminated ·TELEFLEX MEDICAL INC·Product code QEW·January 11, 2022

    5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC containing components: PT-03000, PT-65509-S (PT-65509-S2 alternative), PT-01000-D (PT-01000-D2 alternative) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic dialysis grafts.

    FDA Recall
    Terminated ·TELEFLEX MEDICAL INC·Product code QEW·January 11, 2022

    Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-12709-CA, PT-12709-C, The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic dialysis grafts.

    FDA Recall
    Terminated ·TELEFLEX MEDICAL INC·Product code QEW·January 11, 2022

    Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC containing components: PT-65709-C, PT-03009, PT-65709-HS The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic dialysis grafts.

    FDA Recall
    Terminated ·TELEFLEX MEDICAL INC·Product code QEW·January 11, 2022

    Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65709-C, PT-03009, PT-65709-HFS The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic dialysis grafts.

    FDA Recall
    Terminated ·TELEFLEX MEDICAL INC·Product code QEW·January 11, 2022

    Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic dialysis grafts.

    FDA Recall
    Terminated ·TELEFLEX MEDICAL INC·Product code QEW·January 11, 2022

    Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code GAD·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080080

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781035

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380060

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780085

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023