Duns Number:961027315
Device Description: SP Brand Immu-Sal Saline; For Use in Immunohematological Procedures; For In Vitro Diagnost SP Brand Immu-Sal Saline; For Use in Immunohematological Procedures; For In Vitro Diagnostic Use; For Laboratory Use Only; Not Intended For Internal Use; Not for Infusion, Injection, Irrigation, or Ingestion; 2.5 gal
Catalog Number
B5052-25
Brand Name
SP
Version/Model Number
B5052-25
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)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
PPM
Product Code Name
General purpose reagent
Public Device Record Key
7af3f1c5-f9a6-45b4-9b89-75144a822cd7
Public Version Date
June 29, 2020
Public Version Number
2
DI Record Publish Date
December 27, 2018
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 101686 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 139430 |
| 3 | A medical device with high risk that requires premarket approval | 8 |
| U | Unclassified | 40 |