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Product Description:

BD 305215 Nokor Admix Needles Thin 18 Gauge 1.5 Inch 1000/CS

2018 04 07 17 07 03 405 63 qgld73

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 ColorPink
Hub MaterialPolypropylene
Hub TypeLuer
Needle Gauge18 G
Needle Gauge (m)1.20 mm
Needle Length (in.)1-1/2 in.
Needle Length (m)38.10 mm
Needle Tip TypeBD Nokor
Needle TypeFill
Needle Wall TypeThin wall
Total Shelf Life1825
SterileSterilized product
Type Of BevelBD Nokor
Sterilization MethodRadiation
BPA FreeNot made with BPA
DEHP FreeNot made with DEHP
Latex StatementNot made with natural rubber latex
PVC FreeNot made with PVC
DisposableDisposable product
Single UseProduct 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.

Sterility

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.

Biocompatability

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-UseYes
Prescription Use (Rx)Yes
Over the Counter (OTC)No
KitNo
Combination ProductNo
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)No

Product Packaging Information

Packaging LevelShelfpackEachCase
Quantity10011000
Length116.0 mm451.0 mm
Width88.0 mm206.0 mm
Height98.0 mm129.0 mm
Weight141.9 g1.419 g1.419 kg