BD 305215 - Nokor Admix Needles Thin 18gx1.5" 100/BX, 10 BX/CS


BD 305215 – Nokor Admix Needles Thin 18gx1.5″ 100/BX, 10 BX/CS

305215 – 18 G BD Nokor Admix Needle 1 1/2 in. Thin wall, Sterile, Single use

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.

  • BD Nokor design eliminates clogged cannula, retaining venting capability
  • Vented needles available, designed to reduce internal container pressure

Key Product Features

Hub Color Pink
Hub Material Polypropylene
Hub Type Luer
Needle Gauge 18 G
Needle Gauge (m) 1.20 mm
Needle Length (in.) 1-1/2 in.
Needle Length (m) 38.10 mm
Needle Tip Type BD Nokor
Needle Type Fill
Needle Wall Type Thin wall
Total Shelf Life 1825
Sterile Sterilized product
Type Of Bevel BD Nokor
Sterilization Method Radiation
BPA Free Not made with BPA
DEHP Free Not made with DEHP
Latex Statement Not made with natural rubber latex
PVC Free Not made with PVC
Disposable Disposable product
Single Use Product is for single use only

Regulatory Compliance and Quality System

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.

Quality Control Testing and Release

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.

Device Characteristics

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) No
Device labeled as “Not made with natural rubber latex” No
For Single-Use Yes
Prescription Use (Rx) Yes
Over the Counter (OTC) No
Kit No
Combination Product No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P) No

Product Packaging Information

Packaging Level Shelfpack Each Case
Quantity 100 1 1000
Length 116.0 mm 451.0 mm
Width 88.0 mm 206.0 mm
Height 98.0 mm 129.0 mm
Weight 141.9 g 1.419 g 1.419 kg