Duns Number:153880372
Device Description: sharps container, red vertical entry,8qt
Catalog Number
-
Brand Name
Plasti-Products
Version/Model Number
100285
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
K970398,K970398
Product Code
FMI
Product Code Name
Needle, Hypodermic, Single Lumen
Public Device Record Key
8b4ce61a-a52e-4f6e-b10b-67d83b659327
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
April 15, 2016
Package DI Number
40797876102850
Quantity per Package
20
Contains DI Package
10797876102859
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
case
| 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. | 17 |