Mojo Non Vented Full Face Mask, Medium with Headgear

GUDID 00814747020173

Full face non vented mask for use in positive pressure ventilation.

SLEEPNET, CORP.

CPAP/BPAP face mask, reusable

• Primary Device ID: 00814747020173
• NIH Device Record Key: daf29c8e-cb5d-4885-914b-3748de386837
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mojo Non Vented Full Face Mask, Medium with Headgear
• Version Model Number: 50921
• 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
• Phone: 1-800-742-3646
• Email: xxx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814747020173 [Primary]

FDA Product Code

• CBK: Ventilator, Continuous, Facility Use

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: 2018-03-29
• Device Publish Date: 2015-09-25

On-Brand Devices [Mojo Non Vented Full Face Mask, Medium with Headgear]

• 00814747020173: Full face non vented mask for use in positive pressure ventilation.
• 00814747022979: Full face non vented mask for use in positive pressure ventilation.
• 00814747023730: Full face non vented mask for use in positive pressure ventilation.
• 00814747023976: Full face non vented mask for use in positive pressure ventilation.