Water Phantom, 25 cm

GUDID 10815411020755

NEUROLOGICA CORP.

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• Primary Device ID: 10815411020755
• NIH Device Record Key: 381b4b5a-781c-4e7d-8666-a85f42461405
• Commercial Distribution Discontinuation: 2023-06-15
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Water Phantom, 25 cm
• Version Model Number: 10-01527-001
• Company DUNS: 145008178
• Company Name: NEUROLOGICA CORP.
• 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: true
• Manufacturing Date: true
• 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	10815411020755 [Primary]

FDA Product Code

• JAK: System, X-Ray, Tomography, Computed

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: 2023-06-23
• Device Publish Date: 2023-06-15

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