Floodlight MS Cognitive Test 09341919001

GUDID 07613336193273

Roche Molecular Systems, Inc.

Self-care monitoring/reporting software

• Primary Device ID: 07613336193273
• NIH Device Record Key: de6b2547-a16e-49e1-a1d5-aad979ed00d7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Floodlight MS Cognitive Test
• Version Model Number: 09341919001
• Catalog Number: 09341919001
• Company DUNS: 117676383
• Company Name: Roche Molecular Systems, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• 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	07613336193273 [Primary]

FDA Product Code

• PTY: Computerized Cognitive Assessment Aid, Exempt

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: 2021-01-25
• Device Publish Date: 2021-01-15

On-Brand Devices [Floodlight MS Cognitive Test]

• 07613336193273: 09341919001
• 07613336193266: 09341897001