QLAB Advanced Quantification Software

GUDID 00884838103603

Software Revision 15.5

Philips Ultrasound, Inc.

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• Primary Device ID: 00884838103603
• NIH Device Record Key: 334b6967-4926-44e0-a432-31657ecc001a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QLAB Advanced Quantification Software
• Version Model Number: 989606720441
• 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	00884838103603 [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: 2021-12-22
• Device Publish Date: 2021-12-13

On-Brand Devices [QLAB Advanced Quantification Software]

• 00884838090736: 989605492681
• 00884838084322: 989605465051
• 00884838091672: 989605496481
• 00884838103603: Software Revision 15.5
• 00884838115323: Release 15.6