VISIQ Diagnostic Ultrasound System

GUDID 00884838051133

Philips Ultrasound, Inc.

General-purpose ultrasound imaging system

• Primary Device ID: 00884838051133
• NIH Device Record Key: 97aa5a0a-b49a-40ca-a458-2e931bd1e71b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VISIQ Diagnostic Ultrasound System
• Version Model Number: 989605414421
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838051133 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141369

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: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-12
• Device Publish Date: 2016-08-25

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• 00884838114241 - Affinti 50 Diaagnostic Ultrasound System Circular Edition: 2024-05-13 Software Version 10.0.2
• 00884838114258 - Affinti 70 Diaagnostic Ultrasound System Circular Edition: 2024-05-13 Software Version 10.0.2
• 00884838114203 - EPIQ 7 Diagnostic Ultrasound System Circular Edition: 2024-04-18 10.0.X Circular Edition