Liberant™

GUDID 00763000998615

CATHETER LMT-CT8S LIBERANT 8S

MEDTRONIC, INC.

Thrombectomy suction catheterization kit

• Primary Device ID: 00763000998615
• NIH Device Record Key: 38f1101a-27fc-4835-ae1a-8e96322043b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Liberant™
• Version Model Number: LMT-CT8S
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Inner Diameter: 2.24 Millimeter
• Catheter Length: 50 Centimeter
• Outer Diameter: 2.8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Inner Diameter: 2.24 Millimeter
• Catheter Length: 50 Centimeter
• Outer Diameter: 2.8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Inner Diameter: 2.24 Millimeter
• Catheter Length: 50 Centimeter
• Outer Diameter: 2.8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Inner Diameter: 2.24 Millimeter
• Catheter Length: 50 Centimeter
• Outer Diameter: 2.8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000998615 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K250787

FDA Product Code

• QEW: Peripheral mechanical thrombectomy with aspiration

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: 2025-11-24
• Device Publish Date: 2025-11-16

On-Brand Devices [Liberant™]

• 00763000998646: CATHETER LMT-CT12 LIBERANT 12F
• 00763000998639: CATHETER LMT-CT6 LIBERANT 6F
• 00763000998622: CATHETER LMT-CT8L LIBERANT 8L
• 00763000998615: CATHETER LMT-CT8S LIBERANT 8S
• 00763000849801: CONSOLE LMT-BCU LIBERANT