Marathon

GUDID 00763000400439

CATHETER 105-5056 V06 MARATHON AVM

Micro Therapeutics, Inc.

Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter 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