Duns Number:168560402
Device Description: Single Dip Drug Test, MDMA
Catalog Number
30190
Brand Name
DrugCheck
Version/Model Number
30190
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 26, 2019
Issuing Agency
In HIBCC
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LAF
Product Code Name
Gas Chromatography, Methamphetamine
Public Device Record Key
63653f6e-5c31-4a76-92c7-2a06eb8a889f
Public Version Date
June 10, 2022
Public Version Number
5
DI Record Publish Date
August 29, 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 522 |
U | Unclassified | 2 |