Mojo 2 Full Face Vented Mask, Medium

GUDID 00814747022009

Full face vented mask for use in positive pressure ventilation.

SLEEPNET, CORP.

CPAP/BPAP face mask, reusable

• Primary Device ID: 00814747022009
• NIH Device Record Key: 3b1e0b2d-010c-45c1-8f26-cabf4e5250d9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mojo 2 Full Face Vented Mask, Medium
• Version Model Number: 50818
• Company DUNS: 785635186
• Company Name: SLEEPNET, CORP.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-742-3646
• Email: xxx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814747022009 [Primary]

FDA Product Code

• BZD: Ventilator, Non-Continuous (Respirator)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-12-13
• Device Publish Date: 2019-05-03

On-Brand Devices [Mojo 2 Full Face Vented Mask, Medium]

• 00814747022009: Full face vented mask for use in positive pressure ventilation.
• 00814747023198: Full face vented mask for use in positive pressure ventilation.
• 00814747023778: Full face vented mask for use in positive pressure ventilation.
• 00814747024010: Full face vented mask for use in positive pressure ventilation.