IntelliVue XDS Software 867019

GUDID 00884838123175

IntelliVue XDS Software

Philips Medizin Systeme Böblingen GmbH

Bedside information system application software

• Primary Device ID: 00884838123175
• NIH Device Record Key: 33593a7c-d648-4fe5-9399-405578913468
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IntelliVue XDS Software
• Version Model Number: IntelliVue XDS Software - R
• Catalog Number: 867019
• Company DUNS: 314101143
• Company Name: Philips Medizin Systeme Böblingen GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	00884838123175 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-12-19
• Device Publish Date: 2024-12-11

On-Brand Devices [IntelliVue XDS Software]

• 00884838092099: N
• 00884838123175: IntelliVue XDS Software