GUDID 00721902307294

CABLE 2292 ANALYZER GLOBAL MKT

MEDTRONIC, INC.

Electrical-only medical device connection cable, reusable

• Primary Device ID: 00721902307294
• NIH Device Record Key: 1ee3447b-9dc3-440c-baed-1bdb2f0aa1a9
• Commercial Distribution Discontinuation: 2017-01-05
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 2292
• 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

Operating and Storage Conditions

• Storage Environment Temperature: Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit
• Storage Environment Temperature: Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00721902307294 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P890003

FDA Product Code

• FQM: BANDAGE, ELASTIC
• KRG: Programmer, pacemaker

Sterilization

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

[00721902307294]

Moist Heat or Steam Sterilization;Ethylene Oxide

[00721902307294]

Moist Heat or Steam Sterilization;Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-05-07
• Device Publish Date: 2014-09-23

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