Mirage

GUDID 00763000294120

GUIDEWIRE 103-0608 V08 MIRAGE

Micro Therapeutics, Inc.

Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual

• Primary Device ID: 00763000294120
• NIH Device Record Key: 5013899c-4092-464b-b48e-3ec57ba9ea50
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mirage
• Version Model Number: 103-0608
• 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
• 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
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Stored in a dry place, away from sunlight.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000294120 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193548
• Premarket Notification: K201690

FDA Product Code

• MOF: Guide, wire, catheter, neurovasculature

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: 2020-08-10
• Device Publish Date: 2020-07-31

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• 00847536036260 - PipelineTM Vantage Embolization Device with Shield TechnologyTM: 2024-01-08 STENT PED3-021-250-20 V03 VANTAGE
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