MarathonTM

GUDID 00847536005891

105-5055 MARATHON CATHETER

Micro Therapeutics, Inc.

Vascular microcatheter

• Primary Device ID: 00847536005891
• NIH Device Record Key: 6776766a-3f35-4454-b4eb-43148c28f6f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MarathonTM
• Version Model Number: 105-5055
• 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

Operating and Storage Conditions

• Storage Environment Temperature: Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00847536005891 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093750

FDA Product Code

• KRA: Catheter, continuous flush

Sterilization

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

[00847536005891]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-06-10
• Device Publish Date: 2016-04-05

On-Brand Devices [MarathonTM]

• 00847536005914: 105-5056 MARATHON 165 AVM MICRO CATH
• 00847536005891: 105-5055 MARATHON CATHETER