SPRINTER LEGEND

GUDID 00643169019010

BLN SPL12520WL SPR LEGEND 1.25X20 OTW US

MEDTRONIC, INC.

Coronary angioplasty balloon catheter, basic

• Primary Device ID: 00643169019010
• NIH Device Record Key: 2aec7b0e-fb93-4f85-9642-eabd1e196933
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPRINTER LEGEND
• Version Model Number: SPL12520WL
• Company DUNS: 006261481
• Company Name: MEDTRONIC, 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

Device Dimensions

• Outer Diameter: 1.25 Millimeter
• Outer Diameter: 1.25 Millimeter
• Outer Diameter: 1.25 Millimeter
• Outer Diameter: 1.25 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169019010 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103095

FDA Product Code

• LOX: Catheters, transluminal coronary angioplasty, percutaneous

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-07
• Device Publish Date: 2016-04-28

On-Brand Devices [SPRINTER LEGEND]

• 00643169019010: BLN SPL12520WL SPR LEGEND 1.25X20 OTW US
• 00643169019003: BLN SPL12515WL SPR LEGEND 1.25X15 OTW US
• 00643169018990: BLN SPL12510WL SPR LEGEND 1.25X10 OTW US
• 00643169018983: BLN SPL12506WL SPR LEGEND 1.25X6 OTW US