Duns Number:623214079
Device Description: Captia™ ds/DNA
Catalog Number
2327671
Brand Name
Trinity Biotech
Version/Model Number
2327671
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
K923537
Product Code
LRM
Product Code Name
Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control
Public Device Record Key
f64aaa42-262b-4d7f-9f2c-c73b21a3d3f6
Public Version Date
November 06, 2019
Public Version Number
4
DI Record Publish Date
September 19, 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 | 50 |
2 | A medical device with a moderate to high risk that requires special controls. | 116 |