Duns Number:080935429
Device Description: Pharmaceutical Waste Container,Hinged Lid with Snap Cap
Catalog Number
8820
Brand Name
SharpSafety
Version/Model Number
8820
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
-
Product Code
FMI
Product Code Name
Needle, hypodermic, single lumen
Public Device Record Key
3ebb373f-09bb-445c-a3e2-07c5d3c68919
Public Version Date
February 15, 2019
Public Version Number
7
DI Record Publish Date
September 24, 2016
Package DI Number
20884521019222
Quantity per Package
20
Contains DI Package
30884521019229
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 | 672 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1692 |
| U | Unclassified | 17 |