Orion

GUDID 00836462002579

105-5098-150 ORION 21 MICRO CATHETER

Micro Therapeutics, Inc.

Vascular microcatheter

• Primary Device ID: 00836462002579
• NIH Device Record Key: e9173894-0ef0-4704-91d0-1482766fcd8a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Orion
• Version Model Number: 105-5098-150
• 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	00836462002579 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113289

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: 6
• Public Version Date: 2019-05-17
• Device Publish Date: 2015-10-09

Devices Manufactured by Micro Therapeutics, Inc.

• 00763000448929 - Pipeline TM Flex Embolization Device with Shield Technology TM: 2025-03-19 STENT PED2-325-18 V08 MDR
• 00763000448936 - Pipeline TM Flex Embolization Device with Shield Technology TM: 2025-03-19 STENT PED2-325-20 V08 MDR
• 00763000448943 - Pipeline TM Flex Embolization Device with Shield Technology TM: 2025-03-19 STENT PED2-325-25 V08 MDR
• 00763000448950 - Pipeline TM Flex Embolization Device with Shield Technology TM: 2025-03-19 STENT PED2-325-30 V08 MDR
• 00763000448967 - Pipeline TM Flex Embolization Device with Shield Technology TM: 2025-03-19 STENT PED2-325-35 V08 MDR
• 00763000448974 - Pipeline TM Flex Embolization Device with Shield Technology TM: 2025-03-19 STENT PED2-350-10 V08 MDR
• 00763000449001 - Pipeline TM Flex Embolization Device with Shield Technology TM: 2025-03-19 STENT PED2-350-16 V08 MDR
• 00763000449018 - Pipeline TM Flex Embolization Device with Shield Technology TM: 2025-03-19 STENT PED2-350-18 V08 MDR