BD Pyxis™

GUDID 10885403518348

BD Pyxis™ Enterprise Server ES (v5.5)

CAREFUSION 303, INC.

Anaesthesia cabinet

• Primary Device ID: 10885403518348
• NIH Device Record Key: 39b644a9-07d1-447e-92c8-b957b149b49f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Pyxis™
• Version Model Number: SW-SVR-ES-55
• Company DUNS: 360624720
• Company Name: CAREFUSION 303, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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	10885403518348 [Primary]

FDA Product Code

• BRY: Cabinet, table and tray, anesthesia

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: 2024-12-16
• Device Publish Date: 2024-12-06

On-Brand Devices [BD Pyxis™]

• 10885403520341: BD Pyxis™ Enterprise Server ES (v5.7)
• 10885403520327: MEDSTATION ES V4.7 SW UDI CONTROL MATL
• 10885403518348: BD Pyxis™ Enterprise Server ES (v5.5)