BEUDAMED
    19 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Terminated ×

    C-QUR TacShield Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

    FDA Recall
    Terminated ·Atrium Medical Corporation·Product code FTL·July 19, 2013

    C-QUR Edge Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

    FDA Recall
    Terminated ·Atrium Medical Corporation·Product code FTL·July 19, 2013

    C-QUR V-Patch Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

    FDA Recall
    Terminated ·Atrium Medical Corporation·Product code FTL·July 19, 2013

    C-QUR Mesh (All Sizes, shapes). Intended for use in soft tissue deficiencies.

    FDA Recall
    Terminated ·Atrium Medical Corporation·Product code FTL·July 19, 2013

    Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture

    FDA Enforcement
    Class II ·Terminated·Aesculap Implant Systems LLC·November 2, 2016

    Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture

    FDA Recall
    Terminated ·Aesculap Implant Systems LLC·Product code GAM·August 1, 2016

    C-QUR Mesh (All Sizes, shapes). Intended for use in soft tissue deficiencies.

    FDA Enforcement
    Class II ·Terminated·Atrium Medical Corporation·August 21, 2013

    C-QUR TacShield Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

    FDA Enforcement
    Class II ·Terminated·Atrium Medical Corporation·August 21, 2013

    C-QUR Edge Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

    FDA Enforcement
    Class II ·Terminated·Atrium Medical Corporation·August 21, 2013

    C-QUR V-Patch Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

    FDA Enforcement
    Class II ·Terminated·Atrium Medical Corporation·August 21, 2013

    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

    9x15" Medium Utility Positioner with Cover

    FDA Recall
    Terminated ·Molnlycke Health Care, Inc·Product code OUW·July 26, 2017

    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

    7x10" Small Utility Positioner with Cover

    FDA Recall
    Terminated ·Molnlycke Health Care, Inc·Product code OUW·July 26, 2017

    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