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.

• 00763000518905 - Avigo: 2024-10-29 GUIDEWIRE 103-0606-200 V05 AVIGO MDR
• 00763000518912 - Mirage: 2024-10-29 GUIDEWIRE 103-0608 V09 MIRAGE MDR
• 00763000518929 - X-Pedion: 2024-10-29 GUIDEWIRE 103-0605-200 V09 X-PEDION MDR
• 00763000412487 - Rebar: 2024-08-16 MICRO CATH 105-5081-153 V05 REBAR
• 00847536036215 - PipelineTM Vantage Embolization Device with Shield TechnologyTM: 2024-01-08 STENT PED3-021-250-10 V03 VANTAGE
• 00847536036222 - PipelineTM Vantage Embolization Device with Shield TechnologyTM: 2024-01-08 STENT PED3-021-250-12 V03 VANTAGE
• 00847536036239 - PipelineTM Vantage Embolization Device with Shield TechnologyTM: 2024-01-08 STENT PED3-021-250-14 V03 VANTAGE
• 00847536036246 - PipelineTM Vantage Embolization Device with Shield TechnologyTM: 2024-01-08 STENT PED3-021-250-16 V03 VANTAGE