VICI VENOUS STENT ® SYSTEM H74916120100

GUDID 00852725008171

N/A

Veniti Inc

Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent Iliofemoral vein stent

• Primary Device ID: 00852725008171
• NIH Device Record Key: ea337a1c-d608-4d3c-a6f3-c2c2e880ddf7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VICI VENOUS STENT ® SYSTEM
• Version Model Number: H74916120100
• Catalog Number: H74916120100
• Company DUNS: 079757164
• Company Name: Veniti Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter
• Stent Length: 120 Millimeter
• Stent Diameter: 16 Millimeter
• Length: 100 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00852725008171 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P180013

FDA Product Code

• QAN: Stent, iliac vein

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-17
• Device Publish Date: 2019-05-09

On-Brand Devices [VICI VENOUS STENT ® SYSTEM]

• 00852725008171: N/A
• 00852725008164: N/A
• 00852725008157: N/A
• 00852725008140: N/A
• 00852725008133: N/A
• 00852725008126: N/A
• 00852725008119: N/A
• 00852725008102: N/A
• 00852725008096: N/A