JETi All In One Saline Drive Unit

GUDID WVSDUP2

WALK VASCULAR L.L.C.

Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system Mechanical atherectomy/thrombectomy drive system

• Primary Device ID: WVSDUP2
• NIH Device Record Key: d767acbf-8903-4ff4-a481-c0f572ca3612
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JETi All In One Saline Drive Unit
• Version Model Number: WVSDUP
• Company DUNS: 034774488
• Company Name: WALK VASCULAR L.L.C.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B139WVSDUP0 [Primary]
HIBCC	WVSDUP2 [Package]; Contains: B139WVSDUP0; Package: Case [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201998

FDA Product Code

• QEZ: Aspiration Thrombectomy Catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-08
• Device Publish Date: 2021-02-26

On-Brand Devices [JETi All In One Saline Drive Unit]

• WVSDUP2: WVSDUP
• 08717648351365: WVSDUP