Marathon

GUDID 00763000400439

CATHETER 105-5056 V06 MARATHON AVM

Micro Therapeutics, Inc.

Vascular microcatheter

• Primary Device ID: 00763000400439
• NIH Device Record Key: 7d92ea16-4048-4ff2-9c22-d260e2c1bcec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Marathon
• Version Model Number: 105-5056
• Company DUNS: 826110710
• Company Name: Micro Therapeutics, 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
• 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
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000400439 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K202318

FDA Product Code

• KRA: Catheter, continuous flush

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: 2022-04-18
• Device Publish Date: 2022-04-08

On-Brand Devices [Marathon]

• 00836462002456: Flow Directed Micro Catheter
• 00763000400439: CATHETER 105-5056 V06 MARATHON AVM