JETi Saline Drive Unit

GUDID B139WV03401

WALK VASCULAR L.L.C.

Thrombectomy suction catheter

• Primary Device ID: B139WV03401
• NIH Device Record Key: b2f44b0b-1d6e-4f3e-b2ba-fb83a6bdbf4c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JETi Saline Drive Unit
• Version Model Number: WV0340
• 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	B139WV03401 [Primary]

FDA Product Code

• DXE: Catheter, Embolectomy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-05-16
• Device Publish Date: 2018-01-24

On-Brand Devices [JETi Saline Drive Unit]

• B139WV034011: WV0340-1
• B139WV03401: WV0340
• B139WV00081: WV0008
• B139WV00071: WV0007
• B139WV034511: WV0345-1
• B139WV03451: WV0345