Avigo

GUDID 00763000518905

GUIDEWIRE 103-0606-200 V05 AVIGO MDR

Micro Therapeutics, Inc.

Peripheral vascular guidewire, manual

• Primary Device ID: 00763000518905
• NIH Device Record Key: c906ea31-7e05-4e45-8bc1-d2a01eb20ce0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Avigo
• Version Model Number: 103-0606-200
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000518905 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113454

FDA Product Code

• DQX: Wire, guide, catheter

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: 2024-10-29
• Device Publish Date: 2024-10-21

Devices Manufactured by Micro Therapeutics, Inc.

• 00763000915681 - Riptide™ Aspiration Pump: 2025-08-26 PUMP LMT-RAP V01 LIBERANT
• 00763000980863 - Reservoir: 2025-08-11 RESERVOIR 24106 C NEONT ANGULAR CATH 5CM
• 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