Duns Number:189023351
Device Description: Calibration Verifier
Catalog Number
-
Brand Name
Tru-Zero Bilirubin Standard
Version/Model Number
9456
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
K882059
Product Code
JIT
Product Code Name
Calibrator, Secondary
Public Device Record Key
913a60b6-70c4-4d81-9bf1-53a1b9627c47
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
January 16, 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 | 3 |
2 | A medical device with a moderate to high risk that requires special controls. | 36 |