Preempt Wipes (US)

GUDID 00068460504117

Virox Technologies Inc

Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent

• Primary Device ID: 00068460504117
• NIH Device Record Key: 8b6295dc-a943-49aa-a8e5-04b64c5c652b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Preempt Wipes (US)
• Version Model Number: 6x7
• 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	00068460504117 [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

Devices Manufactured by Virox Technologies Inc

• 10068460506170 - Optim 33 Tb Wipes (CAN): 2022-11-01
• 00068460506494 - Optim 1 (US): 2022-07-22
• 00068460506555 - Optim 1 (US): 2022-07-22
• 10068460506538 - Optim 1 Wipes (US): 2022-07-22
• 00068460506166 - Optim 1 (CAN): 2022-06-03
• 00068460506197 - Optim 33 Tb (CAN): 2022-06-03
• 00068460506227 - Optim 33 Tb (CAN): 2022-06-03
• 00068460506258 - Optim 33 Tb (CAN): 2022-06-03