CB240_Aurora

GUDID 08050593470034

NEURON GUARD SRL

Circulating-fluid localized thermal therapy system control unit

• Primary Device ID: 08050593470034
• NIH Device Record Key: c64b15f5-c85d-40da-bc98-d934a72ed0d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CB240_Aurora
• Version Model Number: CB240A
• Company DUNS: 434359997
• Company Name: NEURON GUARD SRL
• 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: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08050593470034 [Primary]

FDA Product Code

• ILO: Pack, Hot Or Cold, Water Circulating

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: 2024-03-25
• Device Publish Date: 2024-03-15

On-Brand Devices [CB240_Aurora]

• 08050593470034: CB240A
• 08050593470027: CB240C