Duns Number:360624720
Device Description: GRAV SET 20DP V/NV W/CKV 3SS 104-IN
Catalog Number
42493E
Brand Name
Alaris, SmartSite
Version/Model Number
42493E
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FPA
Product Code Name
Set, administration, intravascular
Public Device Record Key
d3dd5d64-59ce-4c68-86a1-f276a9aa5934
Public Version Date
January 20, 2022
Public Version Number
7
DI Record Publish Date
September 22, 2016
Package DI Number
50885403235373
Quantity per Package
100
Contains DI Package
10885403235375
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Shelfpack
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 43 |