Duns Number:005088112
Device Description: Urea Nitrogen Flex® reagent cartridge, 1680 Tests
Catalog Number
K1021
Brand Name
Dimension Vista® Flex® reagent cartridge BUN
Version/Model Number
10445159
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
K051087,K051087
Product Code
CDQ
Product Code Name
UREASE AND GLUTAMIC DEHYDROGENASE, UREA NITROGEN
Public Device Record Key
2398d96d-e078-41d1-bc19-d1f973638605
Public Version Date
November 18, 2021
Public Version Number
6
DI Record Publish Date
September 24, 2016
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 | 363 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 829 |
| 3 | A medical device with high risk that requires premarket approval | 57 |
| U | Unclassified | 7 |