Duns Number:052002029
Device Description: Bifurcated Enteral Extension Set, 70", Low Volume Minibore, Approx. Priming Vol. 1.90 mL, Bifurcated Enteral Extension Set, 70", Low Volume Minibore, Approx. Priming Vol. 1.90 mL, ENFit
Catalog Number
-
Brand Name
Enteral Feeding
Version/Model Number
ENF07019
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 14, 2018
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"
-
For Single-Use
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K895367,K895367
Product Code
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
5032a7ab-3fda-4dcf-b6a8-5de5b0374c82
Public Version Date
August 16, 2018
Public Version Number
4
DI Record Publish Date
September 22, 2016
Package DI Number
20020451100245
Quantity per Package
100
Contains DI Package
00020451100241
Package Discontinue Date
August 14, 2018
Package Status
Not in Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 244 |