Ultima Nasal Cannula 8581-50

GUDID B1408581501

Tubing used to detect airflow in sleep studies.

Braebon Medical Corporation

Gas-sampling/monitoring respiratory tubing, single-use
Primary Device IDB1408581501
NIH Device Record Key2f0cb2ae-2a37-4127-96f6-347de6b9cdaf
Commercial Distribution StatusIn Commercial Distribution
Brand NameUltima Nasal Cannula
Version Model Number8581-50
Catalog Number8581-50
Company DUNS251731105
Company NameBraebon Medical Corporation
Device Count50
DM Exemptfalse
Pre-market Exempttrue
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

Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com
Phone888.462.4841
Emailinfo@braebon.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB14085810 [Unit of Use]
HIBCCB1408581501 [Primary]

FDA Product Code

CATCannula, Nasal, Oxygen

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-18
Device Publish Date2019-11-08

On-Brand Devices [Ultima Nasal Cannula]

B1408582501Tubing used to detect airflow in sleep studies.
B1408581501Tubing used to detect airflow in sleep studies.

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