Duns Number:080456871
Device Description: Nasal ETCO2Cannula, Adult with 14’O2tube and 14’CO2tube with female luer connector and 22 Nasal ETCO2Cannula, Adult with 14’O2tube and 14’CO2tube with female luer connector and 22 mm (I.D.) x 6 mm (O.D.) adaptor
Catalog Number
2812F14-25
Brand Name
AirLife™
Version/Model Number
2812F14-25
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
CCK
Product Code Name
ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE
Public Device Record Key
d5ea0016-8f73-41bc-99b7-cf1f49e576e9
Public Version Date
March 22, 2022
Public Version Number
2
DI Record Publish Date
May 07, 2021
Package DI Number
50190752157246
Quantity per Package
25
Contains DI Package
10190752157248
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1068 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 780 |
| 3 | A medical device with high risk that requires premarket approval | 65 |
| U | Unclassified | 1 |