Duns Number:080935429
Device Description: 1/2 mL Allergy Tray,Permanent Needle
Catalog Number
8881500501
Brand Name
Monoject
Version/Model Number
8881500501
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
December 31, 2025
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FMF
Product Code Name
Syringe, piston
Public Device Record Key
e5af721e-4c86-4208-824e-c2fd837b9743
Public Version Date
May 10, 2022
Public Version Number
6
DI Record Publish Date
September 24, 2016
Package DI Number
20884521013923
Quantity per Package
1000
Contains DI Package
10884521013926
Package Discontinue Date
December 31, 2025
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 |