Duns Number:122561087
Device Description: BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit Contains: 30 each Flu A+ BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit Contains: 30 each Flu A+B Device, RV Reagent D unitized Tubes, Flu A+/B- Control Swabs, Flu B=/A- Control Swabs.
Catalog Number
256045
Brand Name
BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waved kit
Version/Model Number
256045
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
Yes
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
K112277,K132259,K132692,K151291,K152870,K160161
Product Code
GNX
Product Code Name
ANTIGENS, CF (INCLUDING CF CONTROL), INFLUENZA VIRUS A, B, C
Public Device Record Key
bc754aff-f0a1-4a02-9f56-8f54f1b5d1af
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
February 02, 2017
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 | 611 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 614 |
| 3 | A medical device with high risk that requires premarket approval | 36 |
| U | Unclassified | 4 |