Duns Number:023904428
Device Description: Safety Blood Collection Needle 22G x 1 1/4 in (48/box, 50/cs)
Catalog Number
-
Brand Name
McKesson
Version/Model Number
16-NBC22GS
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
K172763,K172763,K172763
Product Code
FMI
Product Code Name
Needle, Hypodermic, Single Lumen
Public Device Record Key
90f3e037-5584-4cd9-9976-0054cfc6a7b4
Public Version Date
October 24, 2022
Public Version Number
4
DI Record Publish Date
June 26, 2019
Package DI Number
40612479244373
Quantity per Package
50
Contains DI Package
20612479244362
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 | 870 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 422 |
| U | Unclassified | 44 |