Preempt Concentrate (US)

GUDID 00068460503929

Virox Technologies Inc

Medical device disinfection agent

• Primary Device ID: 00068460503929
• NIH Device Record Key: e04942d1-becc-4e35-99ec-57ba3d78992f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Preempt Concentrate (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: false
• 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	00068460503929 [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 Concentrate (US)]

• 00068460504360: 55G
• 00068460503929: 1G