Purify O3

GUDID 00851440007049

Purify O3 Elite Sanitizer

RESPONSIVE RESPIRATORY, INC.

Device sterilization/disinfection container, reusable

• Primary Device ID: 00851440007049
• NIH Device Record Key: bcd7faad-13ae-4062-985b-75155d371a97
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Purify O3
• Version Model Number: 190-6100
• Company DUNS: 129132747
• Company Name: RESPONSIVE RESPIRATORY, 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851440007049 [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: 2023-06-20
• Device Publish Date: 2023-06-12

On-Brand Devices [Purify O3]

• 00851440007049: Purify O3 Elite Sanitizer
• 00851440007032: Purify O3 Sanitizer