GUDID 20613994618669

STYLET 628285 US DS KNOB ST

MEDTRONIC, INC.

Catheter stylet

• Primary Device ID: 20613994618669
• NIH Device Record Key: 965723ce-beed-4fef-ac13-e496c8b98790
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 628285
• 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
• 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

Device Dimensions

• Length: 85 Centimeter
• Length: 85 Centimeter
• Length: 85 Centimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter
• Outer Diameter: 0.356 Millimeter
• Length: 85 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994618665 [Primary]
GS1	20613994618669 [Package]; Contains: 00613994618665; Package: PK [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K010906

FDA Product Code

• DRB: STYLET, CATHETER

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-04-01

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