Tunneled dialysis catheters

HeRO Graft Accessory Component Kit

by Artivion, Inc.

An implanted device designed to provide a passage for blood to flow between an artery typically located in an arm, and a peripheral vein, central vein or right atrium, creating a graft fistula that provides blood access for external procedures, especially haemodialysis. It is a synthetic vascular graft/graft assembly with a thin wall and appropriate size (commonly 6 mm diameter) and configuration to facilitate vessel puncturing. It is typically used when it is not possible or convenient to create a direct arteriovenous fistula or for patients who have exhausted peripheral venous access. Disposable devices associated with implantation may be included.

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HeRO Graft Accessory Component Kit models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
HERO 1003— MR ConditionalAvailable

Procedures that use tunneled dialysis catheters

Frequently asked questions

What is HeRO Graft Accessory Component Kit used for?

An implanted device designed to provide a passage for blood to flow between an artery typically located in an arm, and a peripheral vein, central vein or right atrium, creating a graft fistula that provides blood access for external procedures, especially haemodialysis. It is a synthetic vascular graft/graft assembly with a thin wall and appropriate size (commonly 6 mm diameter) and configuration to facilitate vessel puncturing. It is typically used when it is not possible or convenient to create a direct arteriovenous fistula or for patients who have exhausted peripheral venous access. Disposable devices associated with implantation may be included.

Who makes HeRO Graft Accessory Component Kit?

HeRO Graft Accessory Component Kit is made by Artivion, Inc.. It is listed under tunneled dialysis catheters (permcath), dialysis grafts (av grafts and hero) in our device library.

What sizes does HeRO Graft Accessory Component Kit come in?

The FDA device database does not list sizes for HeRO Graft Accessory Component Kit. Check the instructions for use or ask a Artivion, Inc. representative.

Is HeRO Graft Accessory Component Kit MRI safe?

The FDA device database lists HeRO Graft Accessory Component Kit as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is HeRO Graft Accessory Component Kit FDA cleared?

HeRO Graft Accessory Component Kit is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Artivion, Inc. sales representative?

Artivion, Inc. has not listed representatives on LA Vascular yet. Visit the Artivion, Inc. company page for contact details.

Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.

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