NC-2025-8F

GUDID 10620974001376

CO2/O2 Nasal Cannula with 7ft O2 and CO2 tube

Southmedic Incorporated

Nasal oxygen cannula, carbon-dioxide-sampling
Primary Device ID10620974001376
NIH Device Record Keyb4ec2d53-8c29-4cbd-8ac3-4003339f7fd9
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberNC-2025-8F
Catalog NumberNC-2025-8F
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

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100620974001379 [Unit of Use]
GS110620974001376 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CCKANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-03-22
Device Publish Date2016-09-01

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