Duns Number:012789116
Device Description: 22ga x 1" Non-coring Standard Bore Winged Administration Set, 7" Non-DEHP PVC tubing with 22ga x 1" Non-coring Standard Bore Winged Administration Set, 7" Non-DEHP PVC tubing with Pinch Clamp and Female Luer Lock, Latex Free, Lipid Resistant, Approx. Priming Volume: 0.6ml
Catalog Number
-
Brand Name
All-Med, Inc.
Version/Model Number
50-2233
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)
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
fdd9195f-5315-4f64-907c-b437f196026a
Public Version Date
October 23, 2019
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
10816339027710
Quantity per Package
12
Contains DI Package
10816339021305
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 156 |