SENTINEL 040-1754-01

GUDID 10841522129384

SENTINEL 11 / PATHFINDER SL KIT NL

SPACELABS HEALTHCARE (WASHINGTON), INC

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• Primary Device ID: 10841522129384
• NIH Device Record Key: bde139d6-0082-484d-94ac-1787fd475933
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SENTINEL
• Version Model Number: Sentinal 11
• Catalog Number: 040-1754-01
• Company DUNS: 145581588
• Company Name: SPACELABS HEALTHCARE (WASHINGTON), 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841522129384 [Primary]

FDA Product Code

• DQK: Computer, diagnostic, programmable

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-06
• Device Publish Date: 2024-02-27

On-Brand Devices [SENTINEL]

• 10841522104565: DISPLAY,19" LOW COST XPREZZON,94267
• 10841522123214: SENTINEL 10 TEST SYSTEM HL7/DICOM
• 10841522129315: SENTINEL 11 / PATHFINDER SL KIT FR
• 10841522129285: SENTINEL 11 STANDALONE TEST SYSTEM
• 10841522129551: UPGRADE, SENTINEL 10.5 TO 11.5 OR HIGHER
• 10841522129414: SENTINEL 11 RDT TEST SYSTEM
• 10841522129308: SENTINEL 11 HL7 TEST SYSTEM
• 10841522129292: SENTINEL 11 NETWORKED TEST SYSTEM
• 10841522104558: 94267
• 10841522125751: SENTINEL SOFTWARE V11
• 10841522130922: SENTINEL 11 HL7 TEST SYSTEM
• 10841522129384: SENTINEL 11 / PATHFINDER SL KIT NL
• 10841522129339: SENTINEL 11 / PATHFINDER SL KIT IT