Qlab Quantification Software

GUDID 00884838098220

Philips Ultrasound, Inc.

Radiology PACS software

• Primary Device ID: 00884838098220
• NIH Device Record Key: f0401552-4fa4-459b-9ec1-549c0d4f76e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Qlab Quantification Software
• Version Model Number: 989606710071
• 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: true
• Serial Number: false
• 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	00884838098220 [Primary]

FDA Product Code

• QIH: Automated Radiological Image Processing Software

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: 2020-12-18
• Device Publish Date: 2020-12-10

On-Brand Devices [Qlab Quantification Software]

• 00884838086616: Release 10.8.5
• 00884838070837: Release 10.7
• 00884838059788: Release 10.5
• 00884838098220: 989606710071