Duns Number:022721133
Device Description: Patient Cannula Kit
Catalog Number
SO-2076
Brand Name
N/A
Version/Model Number
SO-2076
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
-
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
CAT
Product Code Name
CANNULA, NASAL, OXYGEN
Public Device Record Key
428b964d-dce4-4025-9045-2ea0be7b8487
Public Version Date
March 22, 2022
Public Version Number
3
DI Record Publish Date
February 09, 2018
Package DI Number
10607411951005
Quantity per Package
10
Contains DI Package
00607411951008
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 865 |
2 | A medical device with a moderate to high risk that requires special controls. | 1134 |