Confida™

GUDID 20763000060880

GUIDEWIRE GWBC30 CONFIDA 29L 3YSL

MEDTRONIC, INC.

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 20763000060880
• NIH Device Record Key: 8b5b4e2a-c593-44af-b479-74c4d77031a0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Confida™
• Version Model Number: GWBC30
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: false
• 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

Device Dimensions

• Outer Diameter: 0.89 Millimeter
• Outer Diameter: 0.89 Millimeter
• Outer Diameter: 0.89 Millimeter
• Outer Diameter: 0.89 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000060886 [Primary]
GS1	20763000060880 [Package]; Contains: 00763000060886; Package: PK [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181001

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: 2
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-05-18

On-Brand Devices [Confida™]

• 20643169583737: GUIDEWIRE GWBC30 CONFIDA 29L
• 20643169357055: GUIDEWIRE GWBC30 CONFIDA 26L
• 20763000060880: GUIDEWIRE GWBC30 CONFIDA 29L 3YSL
• 00763000233815: SHEATH CES122230 CONFIDA US 1YSL
• 20763000758640: GUIDEWIRE GWBC30 CONFIDA