Duns Number:120818216
Device Description: NUTRILINE 24 G (2FR) 30 CM CATHETER WITH STYLET AND MICROFLASH INTRODUCER
Catalog Number
1252.030G
Brand Name
Nutriline
Version/Model Number
1252.030G
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"
-
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
K051690,K051690,K051690
Product Code
LJS
Product Code Name
Catheter, intravascular, therapeutic, long-term greater than 30 days
Public Device Record Key
c8d8985e-90d2-44d7-89b2-cad50990047d
Public Version Date
February 19, 2021
Public Version Number
2
DI Record Publish Date
March 13, 2020
Package DI Number
30849884000826
Quantity per Package
10
Contains DI Package
00849884000825
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 | 124 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 833 |