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BD Part #309597 - Syringe 1cc w/Needle SUB-Q 26Gx5/8" 100/BX, 8 BX/CS
309597 - 1 mL BD Slip Tip Syringe with attached needle 26 G x 5/8 in., Sterile, single use
1 mL BD Syringe/Needle Combination, Slip Tip
309597 - 1 mL BD slip-tip syringe with 26 G x 5/8 in. BD PrecisionGlide subcutaneous needle, regular bevel, regular wall. Detachable needle. (100/sp, 800/ca).
Luer slip tip
Our luer slip tip provides a friction-fit connection that requires you to push and twist the syringe tip into the needle hub.
Key Product Features
|Detachable Needle||Product has a detachable needle|
|Needle Gauge||26 G|
|Needle Gauge (m)||0.45 mm|
|Needle Length (in.)||5/8 in.|
|Needle Length (m)||15.88 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||Slip tip|
|Syringe Scale||0.01 mL graduations|
|Total Shelf Life||1825|
|Sterilization Method||EO, 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|
|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.
This product has been evaluated in accordance with ISO 10993 "Biological Evaluation of Medical Devices", and complies with all relevant sections.
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||419.0 mm|
|Width||178.0 mm||362.0 mm|
|Height||154.0 mm||305.0 mm|
|Weight||565.0 g||4.52 kg||5.65 g|