Duns Number:606814960
Device Description: ISE Internal Reference Fill Solution for Olympus AU Series Chemistry Systems
Catalog Number
-
Brand Name
PHOENIX DIAGNOSTICS, INC.
Version/Model Number
21-107
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K020148,K020148
Product Code
CEM
Product Code Name
Electrode, Ion Specific, Potassium
Public Device Record Key
cd8c79cd-d832-4c3f-b241-6d7e8a1e7f49
Public Version Date
March 30, 2020
Public Version Number
4
DI Record Publish Date
January 25, 2018
Package DI Number
10853366007070
Quantity per Package
2
Contains DI Package
00853366007073
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 | 16 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 37 |