Pathfinder SL 98000-01

GUDID 10841522126000

PATHFINDER SL HOLTER ANALYSIS SYSTEM (ENGLISH)

SPACELABS HEALTHCARE (WASHINGTON), INC

Electrocardiographic long-term ambulatory recording analyser

• Primary Device ID: 10841522126000
• NIH Device Record Key: fe418976-4b0c-4927-bf79-222f356e59bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pathfinder SL
• Version Model Number: Pathfinder SL
• Catalog Number: 98000-01
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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	10841522126000 [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: 2023-08-18
• Device Publish Date: 2018-10-08

On-Brand Devices [Pathfinder SL]

• 10841522126000: PATHFINDER SL HOLTER ANALYSIS SYSTEM (ENGLISH)
• 10841522128820: INSTALLATION KIT, PATHFINDER SL 1.9.2