Patient Information Center iX 866389

GUDID 00884838127074

Patient Information Center iX

Philips Medizin Systeme Böblingen GmbH

Centralized patient monitor

• Primary Device ID: 00884838127074
• NIH Device Record Key: 7a6f7742-1976-4458-901a-a4bd1816cc6f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Patient Information Center iX
• Version Model Number: 4.5
• Catalog Number: 866389
• Company DUNS: 314101143
• Company Name: Philips Medizin Systeme Böblingen GmbH
• 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	00884838127074 [Primary]

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: 2025-11-25
• Device Publish Date: 2025-11-17

On-Brand Devices [Patient Information Center iX]

• 00884838127067: Patient Information Center iX
• 00884838127074: Patient Information Center iX