Patient SafetyNet Console

GUDID 00843997012096

MASIMO CORPORATION

Multiple-patient intensive/general healthcare physiologic monitoring system

• Primary Device ID: 00843997012096
• NIH Device Record Key: abf5affa-4b7d-43ff-91ef-3d9be5051aa8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Patient SafetyNet Console
• Version Model Number: 25378
• Company DUNS: 780421038
• Company Name: MASIMO CORPORATION
• 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: 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

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00843997012096 [Primary]

FDA Product Code

• MSX: SYSTEM,NETWORK AND COMMUNICATION,PHYSIOLOGICAL MONITORS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-02-06
• Device Publish Date: 2017-10-12

On-Brand Devices [Patient SafetyNet Console]

• 00843997012096: 25378
• 00843997012089: 25377
• 00843997012072: 25376