GUDID 00681490132367

CABLE 5433A PATIENT ATRIAL 5348

MEDTRONIC, INC.

Electrical-only medical device connection cable, reusable

• Primary Device ID: 00681490132367
• NIH Device Record Key: bfc16ed7-5b40-4bdd-94c4-af770bdf753c
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5433A
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00681490132367 [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: true
• Device Is Sterile: false

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00681490132367]

Moist Heat or Steam Sterilization;Ethylene Oxide

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

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