Duns Number:879187821
Device Description: Reli® Safety Hypodermic Needle, 22G x 1.0", 100ea/bx, 16bx/cs
Catalog Number
SHN22G101
Brand Name
RELI®
Version/Model Number
SHN22G101
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"
Yes
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
FMI
Product Code Name
Needle, Hypodermic, Single Lumen
Public Device Record Key
8032d380-e33b-4b6d-bd01-710b96363bd0
Public Version Date
May 09, 2022
Public Version Number
1
DI Record Publish Date
May 01, 2022
Package DI Number
10386120011254
Quantity per Package
100
Contains DI Package
00386120011257
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Inner Carton
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 7 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 471 |