Duns Number:176458115
Device Description: Francisella Tularensis Antiserum is intended for use as a postive control for Francisella Francisella Tularensis Antiserum is intended for use as a postive control for Francisella Tularensis Antigens.
Catalog Number
-
Brand Name
FRANCISELLA TULARENSIS ANTISERUM
Version/Model Number
1702
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
-
Product Code
GSK
Product Code Name
Antiserum, Francisella Tularensis
Public Device Record Key
96b64fa1-f479-419f-960d-528c59ac4095
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
April 21, 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 | 12 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 22 |