Duns Number:028007698
Device Description: SODIUM CARBONATE REAGENT 10%, 60mL
Catalog Number
35071504
Brand Name
VMA-SKREEN
Version/Model Number
35071504
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 10, 2022
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
-
Product Code
CDF
Product Code Name
Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin
Public Device Record Key
6f0c829c-d9b5-433e-97e6-c20add22dde7
Public Version Date
January 11, 2022
Public Version Number
2
DI Record Publish Date
April 30, 2020
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 | 388 |