Patient Information Center iX 866389

GUDID 00884838121782

Patient Information Center iX

Philips Medical Systems Hsg

Centralized patient monitor

• Primary Device ID: 00884838121782
• NIH Device Record Key: 1caf1ad9-806d-41db-9fb3-e4b88c7ad388
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Patient Information Center iX
• Version Model Number: 4.2
• Catalog Number: 866389
• Company DUNS: 790605856
• Company Name: Philips Medical Systems Hsg
• 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: false
• 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	00884838121782 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211900

FDA Product Code

• MHX: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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: 2023-10-16
• Device Publish Date: 2023-10-06

On-Brand Devices [Patient Information Center iX]

• 00884838104594: Patient Information Center iX
• 00884838112070: Patient Information Center iX
• 00884838121782: Patient Information Center iX
• 00884838122772: Patient Information Center iX