Affiniti 30 Ultrasound Circular Edition

GUDID 00884838113909

Software version 9.X

Philips Ultrasound, Inc.

General-purpose ultrasound imaging system

• Primary Device ID: 00884838113909
• NIH Device Record Key: 9e5ae282-f3b9-4e4d-b539-4d3cc9dc2642
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Affiniti 30 Ultrasound Circular Edition
• Version Model Number: 795121
• 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	00884838113909 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211597

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: 2022-08-10
• Device Publish Date: 2022-08-02

On-Brand Devices [Affiniti 30 Ultrasound Circular Edition]

• 00884838113909: Software version 9.X
• 00884838113893: Software version 7.x