Duns Number:360624720
Device Description: Alaris SmartSite Syringe-Syringe Transfer Device
Catalog Number
MV0450
Brand Name
Alaris, SmartSite
Version/Model Number
MV0450
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
FPA
Product Code Name
Set, administration, intravascular
Public Device Record Key
79385023-3e56-4673-91f9-9945c7bc4a00
Public Version Date
April 27, 2020
Public Version Number
4
DI Record Publish Date
September 22, 2016
Package DI Number
50885403250857
Quantity per Package
2
Contains DI Package
20885403250856
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 | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 43 |