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BD 305062 - Syringe Luer Lock Blunt 5ml 18Gx1.5" 400/CS

BD  # 305062 - Syringe Luer Lock Blunt 5ml 18Gx1.5
Part Number BD 305062
SKU Number CIA3014309
Sell Unit CASE
Ships Within Special Order
List Price $159.50
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Product Description

BD 305062 - Syringe Luer Lock Blunt 5ml 18Gx1.5" 400/CS

5 mL BD Syringe/Needle Combination BD Luer-Lok Tip, 18 G x 1 1/2 in. Blunt Fill Needle

305062 - 5 mL BD Luer-Lok Syringe with attached BD Blunt Fill Needle 18 G x 1 1/2 in., sterile single use, not for skin injection.

BD blunt fill needle are specifically designed to reduce the risk for needlestick injuries during medication preparation. They reduce the need for a broad selection of conventional needles, so you can drive efficiencies and cost reduction through SKU standardization.

Blunt fill needle

Our blunt fill needle is designed for vial access and available with a BD Luer-Lok connection.

Key Product Features

Hub ColorRed
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 TypeBlunt
Needle TypeFill
Needle Wall TypeRegular
Priming Volume0.086 mL
Pyrogen FreeProduct is pyrogen free
Syringe Tip OrientationConcentric
Syringe Tip TypeBD Luer-Lok
Syringe Scale0.2 ml graduations
Total Shelf Life1825
SterileSterilized product
Volumetric Accuracy+/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml
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.


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 E-beam. Sterilization cycle development/validation is performed to 10-6 SAL in accordance with current ISO 11137 guidelines.


All products which are labeled as non-pyrogenic and released for sale by BD have been tested per United States Pharmacopeia (USP) chapter 85 - Bacterial Endotoxins Test and meets limits as specified in chapter 161- Transfusion and Infusion Assemblies and Similar Medical Devices.


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
Combination ProductNo
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)No

Product Packaging Information

Packaging LevelShelfpackEachCase
Length12.123 cm449.58 mm
Width7.123 cm177.8 mm
Height6.123 cm129.54 mm
Weight1.077 kg10.773 g4.309 kg
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