Preempt Plus RTU (US)

GUDID 00068460506104

Virox Technologies Inc

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• Primary Device ID: 00068460506104
• NIH Device Record Key: 22dc9aae-1b7b-4e6b-82f6-960b6606cd74
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Preempt Plus RTU (US)
• Version Model Number: 32oz
• Company DUNS: 255343022
• Company Name: Virox Technologies 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	00068460506104 [Primary]

FDA Product Code

• LRJ: Disinfectant, Medical Devices

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: 2021-10-18
• Device Publish Date: 2021-10-08

On-Brand Devices [Preempt Plus RTU (US)]

• 00068460506142: 1G
• 00068460506104: 32oz