Duns Number:212623821
Device Description: M10142 - Shigella boydii Type 8 Antiserum- 2ml
Catalog Number
M10142
Brand Name
Mast Assure Antisera
Version/Model Number
M10142
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)
Yes
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
-
Product Code
GNB
Product Code Name
Antisera, All Types, Shigella Spp.
Public Device Record Key
e0f8cdf6-95e6-4e4c-bd0b-bbf1e9eae1ff
Public Version Date
March 11, 2019
Public Version Number
1
DI Record Publish Date
February 22, 2019
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 | 10 |
2 | A medical device with a moderate to high risk that requires special controls. | 101 |