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BD Part #309628 - SYRINGE 1CC LL, 800/CS
309628 - 1 mL BD Luer-Lok Syringe sterile, single use polycarbonate
The BD Luer-Lok 1 mL Syringe is ideal for critical clinical applications where avoiding potential needle disengagement, medication leakage, spray or tubing disconnect is crucial. Integral Luer-Lok hub assures secure connection to needles or IV ports. Crystal-clear polycarbonate barrel. Readily visible fluid level.
- Do Not Reuse
- Do Not Reshield Used Needles
- Not made with natural rubber latex
- Not made with DEHP
BD Luer-Lok 1-mL Syringe
Bring Security to Critical Applications
The BD Luer-Lok 1-mL syringe is ideal for critical clinical applications that crucially require you to avoid potential needle disengagement, medication leakage, spray or tubing disconnect.
- BD Luer-Lok thread: The BD Luer-Lok thread provides a secure connection.
- Plunger rod design: Each disposable syringe features a tapered plunger rod for ease of aspiration and a positive plunger rod stop.
- Ease of use: BD syringes feature a clear barrel with bold scale markings.
- Graduation: The 1-mL syringe's scale has 1/100 mL graduation.
BD Luer-Lok Tip
Our BD Luer-Lok tip is generally used for injections requiring a secure connection of the syringe to another device.
Key Product Features
|CE Mark||Product is CE-marked|
|Pyrogen Free||Product is pyrogen free|
|Syringe Tip Orientation||Concentric|
|Syringe Tip Type||BD Luer-Lok|
|Syringe Scale||0.01 mL graduations|
|Total Shelf Life||1825|
|Volumetric Accuracy||+/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml|
|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.
BD Products which are CE marked comply with Medical Devices Directive 93/42/EEC and are manufactured within production facilities that comply with the international standard ISO 13485: Quality Systems - Medical Devices - Requirements For regulatory purposes.
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. 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||232.0 mm||465.0 mm|
|Width||149.0 mm||298.0 mm|
|Height||159.0 mm||319.0 mm|
|Weight||850.0 g||6.8 kg||8.5 g|