WorkMate™ Unity™ H702321

GUDID 05415067023216

Software Upgrade Kit

ST. JUDE MEDICAL, INC.

Cardiac catheterization monitoring system

• Primary Device ID: 05415067023216
• NIH Device Record Key: cc62ea90-01e7-4099-8293-778f8bdfa7ec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WorkMate™ Unity™
• Version Model Number: Module
• Catalog Number: H702321
• Company DUNS: 149818952
• Company Name: ST. JUDE MEDICAL, 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: true
• 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(855)478-5833
• Email: customerservice@sjm.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Do not use if package is damaged.

Device Identifiers

Device Issuing Agency	Device ID
GS1	05415067023216 [Primary]

FDA Product Code

• DQK: COMPUTER, DIAGNOSTIC, PROGRAMMABLE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-13

On-Brand Devices [WorkMate™ Unity™]

• 05415067023216: Software Upgrade Kit
• 05415067035608: Software Installation
• 05415067035578: Software Installation
• 05415067035561: Software Installation
• 05415067047229: Software Upgrade, 10 Licenses
• 05415067047199: Software Upgrade Site License
• 05415067047168: Module Software Upgrade Single License