Lumify Diagnostic Ultrasound System

GUDID 00884838122116

Android 5.0

Philips Ultrasound, Inc.

General-purpose ultrasound imaging system

• Primary Device ID: 00884838122116
• NIH Device Record Key: 75960e65-e291-4a6c-bf87-8370da58ff0f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumify Diagnostic Ultrasound System
• Version Model Number: 795005
• Company DUNS: 063377717
• Company Name: Philips Ultrasound, Inc.
• 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	00884838122116 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223771

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-08
• Device Publish Date: 2024-03-29

On-Brand Devices [Lumify Diagnostic Ultrasound System]

• 00884838100121: 795005
• 00884838122116: Android 5.0