Marksman

GUDID 00836462014077

FA-55150-1030 MARKSMAN CATHETER 150CM

Micro Therapeutics, Inc.

Vascular microcatheter

• Primary Device ID: 00836462014077
• NIH Device Record Key: 54d03e6c-4ebb-421b-9cb4-9e37c7c12011
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Marksman
• Version Model Number: FA-55150-1030
• 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

Device Dimensions

• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing Agency	Device ID
GS1	00836462014077 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091559

FDA Product Code

• KRA: Catheter, continuous flush

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2019-06-27
• Device Publish Date: 2015-10-12

On-Brand Devices [Marksman]

• 00836462014077: FA-55150-1030 MARKSMAN CATHETER 150CM
• 00836462014060: FA-55135-1030 MARKSMAN CATHETER 135CM
• 00836462014053: FA-55105-1015 MARKSMAN CATHETER 105CM