Duns Number:084963177
Device Description: Artisan User Fillable Dispenser #1
Catalog Number
-
Brand Name
Artisan User Fillable Dispenser #1
Version/Model Number
AR185
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 19, 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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KPA
Product Code Name
Slide stainer, automated
Public Device Record Key
e09e8ebb-20a3-4d03-87c1-0f9432605599
Public Version Date
July 20, 2022
Public Version Number
4
DI Record Publish Date
September 17, 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 | 1076 |
2 | A medical device with a moderate to high risk that requires special controls. | 16 |
3 | A medical device with high risk that requires premarket approval | 8 |