Preempt RTU (US)

GUDID 00068460504629

Virox Technologies Inc

Medical device disinfection agent

• Primary Device ID: 00068460504629
• NIH Device Record Key: 45419d6a-7592-4a0e-b21c-fd977a5f35ff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Preempt RTU (US)
• Version Model Number: 1G
• 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	00068460504629 [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 RTU (US)]

• 00068460504629: 1G
• 00068460504612: 32oz