Duns Number:080278407
Device Description: Areta 12 Panel Drug Test Cup (5 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO,MTD,MDMA,P Areta 12 Panel Drug Test Cup (5 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO,MTD,MDMA,PCP
Catalog Number
ACDOA-6125B-5
Brand Name
Areta Multi-Drug Test Cup (5 tests kit)
Version/Model Number
ACDOA-6125B
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K133968,K133968,K133968
Product Code
CAF
Product Code Name
Nebulizer (Direct Patient Interface)
Public Device Record Key
fc8ed9a3-1198-4cd8-abbc-1b4ae1d3ea9c
Public Version Date
July 25, 2022
Public Version Number
7
DI Record Publish Date
June 26, 2018
Package DI Number
10855944007281
Quantity per Package
16
Contains DI Package
00855944007284
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 4 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 47 |