Primary Device ID | B1400582MCO2PED501 |
NIH Device Record Key | 8c3b04d7-7c61-4dd1-a1d6-7ec33bb0f2bf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ultima Divided Nasal Cannula + Filter, Pediatric |
Version Model Number | 0582MCO2-PED-50 |
Catalog Number | 0582MCO2-PED-50 |
Company DUNS | 251731105 |
Company Name | Braebon Medical Corporation |
Device Count | 50 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com | |
Phone | 888.462.4841 |
info@braebon.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B1400582MCO2PED0 [Unit of Use] |
HIBCC | B1400582MCO2PED501 [Primary] |
CAT | Cannula, Nasal, Oxygen |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-04 |
Device Publish Date | 2019-10-25 |
B1400582MCO2PED501 | Tubing used to detect airflow in sleep studies. |
B1400582CO2PED501 | Tubing used to detect airflow in sleep studies. |