RD SedLine

GUDID 10843997011775

EEG Sensor Adult

MASIMO CORPORATION

Patient monitoring system module, electroencephalographic

• Primary Device ID: 10843997011775
• NIH Device Record Key: 1e0bf05e-2328-473a-9b2c-42de2fb2aef2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RD SedLine
• Version Model Number: 4248
• Company DUNS: 780421038
• Company Name: MASIMO CORPORATION
• Device Count: 25
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(949)297-7498
• Email: TechService-US@masimo.com

Operating and Storage Conditions

• Handling Environment Temperature: Between 10 Degrees Celsius and 32 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00843997011778 [Unit of Use]
GS1	10843997011775 [Primary]

FDA Product Code

• GXY: ELECTRODE, CUTANEOUS

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: 2019-10-01
• Device Publish Date: 2019-09-23

On-Brand Devices [RD SedLine]

• 10843997011775: EEG Sensor Adult
• 00843997012485: RD Sedline Patient Cable
• 00843997000581: RD SedLine EEG Sensor, Pediatric
• 00843997012805: RD Sedline EEG Sensor Pediatric