Duns Number:088013219
Catalog Number
-
Brand Name
Fresenius Kabi Apheresis Needle with masterguard Anti-Stick Needle Protector
Version/Model Number
4R2441
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
FIE
Product Code Name
Needle, Fistula
Public Device Record Key
722eea5b-9694-4109-af30-f661ea7c1a01
Public Version Date
April 07, 2021
Public Version Number
2
DI Record Publish Date
June 09, 2020
Package DI Number
10842289102634
Quantity per Package
250
Contains DI Package
00842289102637
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Shipping Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 211 |