Guidewires
Morpheus
A collection of nonimplantable, invasive devices intended to provide percutaneous vascular access to enable introduction of a catheter (not included) into the vascular system. It includes a non-steerable introducer sheath with an inner obturator/dilator, and typically an additional access device(s) [e.g., guidewire, introducer needle, syringe, additional dilators] which may include a haemostatic valve to control blood loss, usually to enable arterial access. This is a single-use device.
Morpheus models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 06507210 | Outer Diameter 0.018 in; Length 80 cm | Not stated | Available |
| 06507211 | Length 130 cm; Outer Diameter 0.018 in | Not stated | Available |
| 06507212 | Length 80 cm; Outer Diameter 0.018 in | Not stated | Available |
| 06507213 | Outer Diameter 0.018 in; Length 130 cm | Not stated | Available |
FDA clearances
- 510(k) K051655 September 2005
Procedures that use guidewires
Frequently asked questions
What is Morpheus used for?
A collection of nonimplantable, invasive devices intended to provide percutaneous vascular access to enable introduction of a catheter (not included) into the vascular system. It includes a non-steerable introducer sheath with an inner obturator/dilator, and typically an additional access device(s) [e.g., guidewire, introducer needle, syringe, additional dilators] which may include a haemostatic valve to control blood loss, usually to enable arterial access. This is a single-use device.
Who makes Morpheus?
Morpheus is made by AngioDynamics, Inc.. It is listed under guidewires in our device library.
What sizes does Morpheus come in?
Sizes listed for Morpheus: Length: 80–130 cm; Outer Diameter: 0.02 in. Confirm availability with the manufacturer's instructions for use.
Is Morpheus MRI safe?
The FDA device database entry for Morpheus does not state its MRI safety status. Check the labeling before MRI.
Is Morpheus FDA cleared?
Morpheus is covered by FDA submission K051655.
How do I contact a AngioDynamics, Inc. sales representative?
AngioDynamics, Inc. has not listed representatives on LA Vascular yet. Visit the AngioDynamics, 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.