GUDID 20613994524274

POUCH 5409 DISP 5PK US

MEDTRONIC, INC.

Instrument management bag, non-sterile Instrument management bag, non-sterile Instrument management bag Instrument management bag Instrument management bag Instrument management bag Instrument management bag

• Primary Device ID: 20613994524274
• NIH Device Record Key: 4bf782b1-a430-43af-91ac-14fe41ebd197
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5409
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 5
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994524270 [Unit of Use]
GS1	20613994524274 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P820003

FDA Product Code

• LWP: Implantable pulse generator, pacemaker (non-CRT)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2014-09-23

Devices Manufactured by MEDTRONIC, INC.

• 00763000897642 - Launcher™: 2024-05-15 CATHETER LA6ALR12A LA 6F 110CM ALR12
• 00763000897659 - Launcher™: 2024-05-15 CATHETER LA6AR10A LA 6F 110CM AR10
• 00763000897666 - Launcher™: 2024-05-15 CATHETER LA6AR20A LA 6F 110CM AR20
• 00763000897673 - Launcher™: 2024-05-15 CATHETER LA6AL30A LA 6F 110CM AL30
• 00763000897680 - Launcher™: 2024-05-15 CATHETER LA6AL40A LA 6F 110CM AL40
• 00763000897697 - Launcher™: 2024-05-15 CATHETER LA6HSIA LA 6F 110CM HSI
• 00763000897703 - Launcher™: 2024-05-15 CATHETER LA6HSIIA LA 6F 110CM HSII
• 00763000897710 - Launcher™: 2024-05-15 CATHETER LA6JCL40A LA 6F 110CM JCL40