BD 309657 - Luer-Lok Syringe Only 3cc 200/BX, 4 BX/CS
BD Luer-Lok Syringe
309657 - 3 mL BD Luer-Lok Syringe Sterile, Single use
- Sterile
- Do Not Reuse
- Do Not Reshield Used Needles
- Not made with natural rubber latex
- Not made with DEHP
BD Luer-Lok Tip
Bring Security to Critical Applications
- 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.
Key Product Features
| Parenteral | Parenteral product |
| 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 |
| Sterile | Sterilized product |
| Volumetric Accuracy | +/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml |
| Sterilization Method | Radiation,EO |
| 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 |
| Disposable | Disposable product |
| 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.
Sterility
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.
Biocompatability
This product has been evaluated in accordance with ISO 10993 "Biological Evaluation of Medical Devices", and complies with all relevant sections.
Pyrogenicity
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.
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-Use | Yes |
| Prescription Use (Rx) | Yes |
| Over the Counter (OTC) | No |
| Kit | No |
| Combination Product | No |
| Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P) | No |
Product Packaging Information
| Packaging Level | Shelfpack | Case | Each |
| Quantity | 200 | 800 | 1 |
| Length | 30.0 cm | 30.0 cm | |
| Width | 19.0 cm | 38.0 cm | |
| Height | 17.3 cm | 34.6 cm | |
| Weight | 1.034 kg | 4.136 kg | 5.17 g |
