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 CPAP/BPAP face mask, reusable
Primary Device ID00814747020173
NIH Device Record Keydaf29c8e-cb5d-4885-914b-3748de386837
Commercial Distribution StatusIn Commercial Distribution
Brand NameMojo Non Vented Full Face Mask, Medium with Headgear
Version Model Number50921
Company DUNS785635186
Company NameSLEEPNET, CORP.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-742-3646
Emailxxx@xx.xx
Phone1-800-742-3646
Emailxxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100814747020173 [Primary]

FDA Product Code

CBKVentilator, Continuous, Facility Use

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-09-25

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

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

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.