The BD Nokor needle design features a cannula side port to place fluid on the side wall of a container during reconstitution. Some drug manufacturers recommend this to help reduce foaming or spray of powdered medication.
|Needle Gauge (m)
|Needle Length (in.)
|Needle Length (m)
|Needle Tip Type
|Needle Wall Type
|Total Shelf Life
|Type Of Bevel
|Not made with BPA
|Not made with DEHP
|Not made with natural rubber latex
|Not made with PVC
|Product is for single use only
BD Products comply with the regulatory requirements of the region in which these are sold and manufactured.
All products which are labeled as #sterile# and released for sale by BD are certified to be sterile as long as the package is unopened and undamaged. For those products labeled #sterile fluid path#, only the fluid path is sterile. This product is primarily sterilized via Gamma radiation. Sterilization cycle development/validation is performed to 10-6 SAL in accordance with current ISO 11137 guidelines.
This product has been evaluated in accordance with ISO 10993 “Biological Evaluation of Medical Devices”, and complies with all relevant sections.
Representative production samples are collected and inspected in accordance with current applicable product specifications. Inspection records are reviewed and signed off by qualified personnel for product release. The released devices meet applicable BD product specifications.
|What MRI safety information does the labeling contain?
|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”
|Prescription Use (Rx)
|Over the Counter (OTC)
|Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)