309582 – 3 mL BD Luer-Lok Syringe with attached needle 25 G x 1.5 in., Sterile, Single use
3cc, 25g x 1.5″, Standard Syringes with Needle
3mL Luer-Lok Syringe With 25G x 1.5″ PrecisionGlide Needle Combination. Regular bevel, regular wall. Detachable needle. World’s sharpest needle is combined with BD’s clear barrel featuring bold scale. Syringes have positive plunger rod stop and tapered plunger rod design.
BD conventional syringes are available with and without an attached needle. BD syringe-needle combinations feature a clear barrel with a bold scale. Disposable syringes with a BD Luer-Lok tip, luer slip tip or eccentric luer slip tip can be fitted with either a conventional needle or safety needle.
Key Product Features
|Detachable Needle||Product has a detachable needle|
|Needle Gauge||25 G|
|Needle Gauge (m)||0.50 mm|
|Needle Length (in.)||1.5 in.|
|Needle Length (m)||38.10 mm|
|Needle Tip Type||Regular|
|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||0.1 mL graduations|
|Total Shelf Life||1825|
|Volumetric Accuracy||+/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml|
|Sterilization Method||EO, Radiation|
|Not made with BPA||BPA Free|
|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 10-6SAL 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.
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||210.0 mm||414.0 mm|
|Width||188 mm||380 mm|
|Height||170 mm||330 mm|
|Weight||700.0 g||7.0 g||5.6 kg|