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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
|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||Blunt|
|Needle Wall Type||Regular|
|Priming Volume||0.086 mL|
|Pyrogen Free||Product is pyrogen free|
|Syringe Tip Orientation||Concentric|
|Syringe Tip Type||BD Luer-Lok|
|Syringe Scale||0.2 ml graduations|
|Total Shelf Life||1825|
|Volumetric Accuracy||+/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml|
|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|
|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 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.
|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|
|Prescription Use (Rx)||Yes|
|Over the Counter (OTC)||No|
|Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)||No|
Product Packaging Information
|Length||12.123 cm||449.58 mm|
|Width||7.123 cm||177.8 mm|
|Height||6.123 cm||129.54 mm|
|Weight||1.077 kg||10.773 g||4.309 kg|