Lumify USB-C to USB-C Transducer cable

GUDID 00884838125964

Lumify USB-C to USB-C Transducer cable

Philips Ultrasound LLC

Electrical-only medical device connection cable, reusable

• Primary Device ID: 00884838125964
• NIH Device Record Key: 5d848aea-a6cd-4882-bd05-8964bd67265e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumify USB-C to USB-C Transducer cable
• Version Model Number: 300014217991
• Company DUNS: 063377717
• Company Name: Philips Ultrasound LLC
• 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: 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	00884838125964 [Primary]

FDA Product Code

• IYO: System, Imaging, Pulsed Echo, Ultrasonic

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: 2025-07-22
• Device Publish Date: 2025-07-14

Devices Manufactured by Philips Ultrasound LLC

• 00884838129276 - Ultrasound Workspace: 2025-09-08 Device Model: 300013759461
• 00884838123625 - Ultrasound System 5500CV: 2025-07-28 As part of SW 2.0
• 00884838123632 - Ultrasound System 5500P: 2025-07-28 Part of SW 2.0
• 00884838123649 - Ultrasound System 5500W: 2025-07-28 Part of SW 2.0
• 00884838123656 - Ultrasound System 5300G: 2025-07-28 Part of SW 2.0
• 00884838123663 - Ultrasound System 5300W: 2025-07-28 As part of SW 2.0
• 00884838123670 - Ultrasound System 5300P: 2025-07-28 As part of SW 2.0
• 00884838123687 - Ultrasound System 5500G: 2025-07-28 As part of SW 2.0