BEUDAMED
    3,570 results · 23ms · Sources: EU EUDAMED, US FDA

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    Enzyme Linked Immunoabsorbent Assay, Rubeola Igm

    FDA classification
    FDA Class 1 ·Enzyme Linked Immunoabsorbent Assay, Rubeola Igm

    1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard, With suture Plugs, (01)00801741026720; 2. PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single- Lumen Venous Catheter, REF: 1709601, Air Guard, Without Suture Plugs, (01)00801741026737; 3. PowerPort Implantable Port with Pre-Attached 9.6F Open-Ended Single-Lumen Venous Catheter, REF: 1759600 Air Guard, With Suture Plugs, (01)00801741026850 Product Usage: Bard implantable ports are 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.

    FDA Recall
    Terminated ·Bard Peripheral Vascular Inc·Product code LJT·October 1, 2019

    1. X-Port isp M.R.I Implantable Port, with Pre-Attached 9.6 F Open-Ended Single-Lumen Venous Catheter, REF:0607550, UDI:(01)00801741026195 2. X-Port isp M.R.I. Implantable Port, with Attachable 9.6F Open-Ended Single-Lumen Venous Catheter, REF: 0657525, UDI:(01)00801741026379 Product Usage: Bard implantable ports are 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.

    FDA Recall
    Terminated ·Bard Peripheral Vascular Inc·Product code LJT·October 1, 2019

    1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, REF: 1809600, UDI: (01)00801741027130 ; 2. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter Without Suture Plugs, REF: 1809601, UDI: (01)00801741027147; 3. PowerPort M.R.I. Implantable Port With Pre-Attached 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, REF: 1859600, UDI: (01)00801741027208 Product Usage: Bard implantable ports are 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.

    FDA Recall
    Terminated ·Bard Peripheral Vascular Inc·Product code LJT·October 1, 2019

    1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, Ref: 1809660, UDI: (01)00801741027154 2. PowerPort isp M.R.I. Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter Without Suture Plugs, Ref: 1809661, UDI: (01)00801741027161 3. PowerPort isp M.R.I. Implantable Port with Pre-Attached 9.6F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, Ref: 1859660, UDI: (01)00801741027222 4. PowerPort isp M.R.I. Implantable Port with Pre-Attached 9.6 F Open-Ended Single-Lumen Venous Catheter without Suture Plugs, Ref: 1859661, UDI: (01)00801741027239 Product Usage: Bard implantable ports are 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.

    FDA Recall
    Terminated ·Bard Peripheral Vascular Inc·Product code LJT·October 1, 2019

    Assay,Enzyme Linked Immunosorbent,Parvovirus B19 Igm

    FDA classification
    FDA Class 3 ·Assay,Enzyme Linked Immunosorbent,Parvovirus B19 Igm

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA classification
    FDA Class 2 ·Hepatitis A Test (Antibody And Igm Antibody)

    Igm (Mu Chain Specific), Antigen, Antiserum, Control

    FDA classification
    FDA Class 2 ·Igm (Mu Chain Specific), Antigen, Antiserum, Control

    Multiplex Flow Immunoassay, T. Gondii, Rubella, Cmv Igm

    FDA classification
    FDA Class 2 ·Multiplex Flow Immunoassay, T. Gondii, Rubella, Cmv Igm

    Test, Qualitative, Detection Of Dengue Igm And Igg Antibodies

    FDA classification
    FDA Not Classified ·Test, Qualitative, Detection Of Dengue Igm And Igg Antibodies