Duns Number:023904428
Device Description: Safety Hypodermic Needles GLIDE Thin Wall 21G x 1 in (50/bx, 10/cs)
Catalog Number
-
Brand Name
McKesson
Version/Model Number
306617
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
K951254,K951254,K951254
Product Code
FMI
Product Code Name
Needle, Hypodermic, Single Lumen
Public Device Record Key
500e83e7-ad49-413d-b64e-e1c826e8d8f4
Public Version Date
April 19, 2022
Public Version Number
1
DI Record Publish Date
April 11, 2022
Package DI Number
20612479262489
Quantity per Package
50
Contains DI Package
10612479262475
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 870 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 422 |
| U | Unclassified | 44 |