Duns Number:988402590
Device Description: INJECTOR LUER LOCK N35C
Catalog Number
515004
Brand Name
BD PhaSeal
Version/Model Number
515004
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
ONB
Product Code Name
Closed antineoplastic and hazardous drug reconstitution and transfer system
Public Device Record Key
bbbe0297-6257-4892-93ed-1d1ccda2543e
Public Version Date
October 23, 2019
Public Version Number
3
DI Record Publish Date
September 19, 2016
Package DI Number
50382905150048
Quantity per Package
4
Contains DI Package
30382905150044
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 9 |