OAT-4025-8

GUDID 10620974000638

OxyTrach Mask Adult O2 Aerosol with Nebulizer Kit

Southmedic Incorporated

Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask Vortex oxygen face mask
Primary Device ID10620974000638
NIH Device Record Keyc267627a-80db-411d-80d6-001d69bf60e5
Commercial Distribution Discontinuation2020-12-18
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberOAT-4025-8
Catalog NumberOAT-4025-8
Company DUNS246848147
Company NameSouthmedic Incorporated
Device Count25
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com
Phone+1(705)726-9383
Emailcustserv@southmedic.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100620974000631 [Unit of Use]
GS110620974000638 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CAFNEBULIZER (DIRECT PATIENT INTERFACE)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-12-14
Device Publish Date2016-09-01

Devices Manufactured by Southmedic Incorporated

00620974003687 - Oxy2Mask O2/EtCO22024-02-05 Oxy2Mask O2/EtCO2 Plus
00620974003090 - Oxy2Pro2023-12-11 Oxy2Pro Procedural Plus Mask with Female Luer
00620974003106 - Oxy2Pro2023-12-11 Oxy2Pro Procedural Plus Mask with Male Luer
00620974003120 - Oxy2Mask O2/EtCO22023-12-11 Oxy2Mask O2/EtCO2 Kid
00620974003137 - Oxy2Mask O2/EtCO22023-12-11 Oxy2Mask O2/EtCO2 Kid Mask with Microsteam connector
00620974003151 - Oxy2Mask O2/EtCO22023-12-11 Oxy2Mask O2/EtCO2 Adult
00620974003168 - Oxy2Mask O2/EtCO22023-12-11 Oxy2Mask O2/EtCO2 Adult
00620974003175 - Oxy2Mask O2/EtCO22023-12-11 Oxy2Mask O2/EtCO2 Adult

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