Liberant™

Basic Information

• Brand Name: Liberant™
• Primary DI: 00763000849801
• Version / Model: LMT-BCU
• Company Name: MEDTRONIC, INC.
• Labeler DUNS: 006261481
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2025-11-16
• Public Version: 1
• Public Version Date: 2025-11-24
• Public Version Status: New
• Public Device Record Key: 532d92c1-d1df-4aae-aedc-95d4f3e66561

Device Description

CONSOLE LMT-BCU LIBERANT

Device Characteristics

• Single Use: No
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: MR Unsafe
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: Yes
• Has Lot/Batch Number: No
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
QEW	Peripheral mechanical thrombectomy with aspiration	Cardiovascular	870.5150	2

GMDN Terms

Code	Name	Definition	Implantable	Status
66970	Thrombectomy blood aspiration regulator	A benchtop device designed to be used during a thrombectomy procedure to minimize excessive blood loss by detecting aspirated blood vs clotted blood (thrombus) flow rates via its sensor and automatically adjusting its integral aspiration valves. It consists of a small electrically-powered unit installed within the aspiration line between a suction pump and a thrombectomy suction catheter.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00763000849801	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]

Premarket Submissions

Submission Number	Supplement Number
K250787	000

Storage Conditions

• Type: Special Storage Condition, Specify
• Special Conditions: Keep dry