Affiniti 30 Diagnostic Ultrasound System

GUDID 00884838124929

Affiniti 30 Diagnostic Ultrasound System

Philips Ultrasound LLC

General-purpose ultrasound imaging system

• Primary Device ID: 00884838124929
• NIH Device Record Key: 388bdabe-6b08-412d-a22f-b0dce5215a27
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Affiniti 30 Diagnostic Ultrasound System
• Version Model Number: 795180
• Company DUNS: 063377717
• Company Name: Philips Ultrasound LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	00884838124929 [Primary]

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: 2026-01-16
• Device Publish Date: 2026-01-08

On-Brand Devices [Affiniti 30 Diagnostic Ultrasound System]

• 00884838124929: Affiniti 30 Diagnostic Ultrasound System
• 00884838112988: 10.X