Duns Number:276816717
Device Description: VIDAS ® D-Dimer Exclusion II™ is an automated quantitative test for use on the VIDAS instr VIDAS ® D-Dimer Exclusion II™ is an automated quantitative test for use on the VIDAS instruments indicated for use in conjunction with a clinical model to exclude DVT and PE.
Catalog Number
-
Brand Name
VIDAS® D-Dimer Exclusion II ™
Version/Model Number
30455-01
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
K141133
Product Code
DAP
Product Code Name
Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control
Public Device Record Key
259afd9d-f72e-4c22-a54c-f52048d03d51
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
August 31, 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 | 82 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 156 |
| 3 | A medical device with high risk that requires premarket approval | 3 |