- Physicians Office Resource

STENT GRAFT VNMF2520C185TU VAL NAV FF TP
Valiant Navion™ - VNMF2520C185TU

Device Description

A non-bioabsorbable tubular device intended to be implanted within the descending thoracic aorta to repair the vessel [includes repair of thoracic aortic aneurysm (TAA), traumatic transsections/dissections, fistulae, penetrating ulcers]; it is not intended for implantation within the aortic arch. It is typically made of a metal alloy [e.g., nickel-titanium alloy (Nitinol)] that forms an outer mesh structure with an inner synthetic polymer tube (endovascular graft) and is typically designed as a single continuous tube which may be used in singular and/or modular configurations. It is intended for percutaneous introduction; disposable delivery device (e.g., balloon catheter) may be included.

Environmental Conditions

Special Storage Condition, Specify

Store the system at room temperature in a dark, dry place.

Device Sizes

Stent Graft Proximal Diameter 25 MM

Stent Graft Length (Covered) 185 MM

Stent Graft Distal Diameter 20 MM

Stent Graft Proximal Diameter 25 MM
Stent Graft Length (Covered) 185 MM
Stent Graft Distal Diameter 20 MM

Device Sterilization

Device Sterile: True

Sterilization Prior To Use: False

Sterilization Methods: No Data Available

Product Codes

Code: MIH

Device Name: System, Endovascular Graft, Aortic Aneurysm Treatment

Device Class: 3

Physical State: N/A

Definition: N/A

Submission Type ID: 2

Review Panel: CV

Review Code: N/A

Technical Method: N

Gmp Exempt Flag: N/A

Life Sustain Support Flag: N

Unclassified Reason: N/A

Implant Flag: Y

Target Area: N/A

Regulation Number: N/A

Third Party Flag: N

Medical Specialty: N/A

Device Identifiers

Device Id: 00763000100827

Device Type: Primary

DeviceId Issuing Agency: GS1

Contains DI Number: N/A

Package Quantity: N/A

Package Discontinue Date: N/A

Package Status: N/A

Package Type: N/A

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