Lumify System Bundle

GUDID 00884838085930

Philips Ultrasound, Inc.

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 00884838085930
• NIH Device Record Key: 71502ab5-8867-4551-949e-c818c1a26310
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumify System Bundle
• Version Model Number: 989605477201
• Company DUNS: 063377717
• Company Name: Philips Ultrasound, Inc.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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	00884838085930 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162549

FDA Product Code

• IYN: System, imaging, pulsed doppler, ultrasonic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-04-07

On-Brand Devices [Lumify System Bundle]

• 00884838085930: 989605477201
• 00884838098176: 795006