Duns Number:790074793
Device Description: Hemoglobin A1c assay, Ultra2 Buffer B Reagent - 3.8L
Catalog Number
01-03-0012
Brand Name
Trinity Biotech
Version/Model Number
Ultra2 Buffer B Reagent - 3.8L
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K891235
Product Code
LCP
Product Code Name
Assay, Glycosylated Hemoglobin
Public Device Record Key
2cb1b4d5-3ce2-4a6f-9967-591797f176e2
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 06, 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 | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 52 |