BD 309680 Tray Convenience Bulk STE

$195.88

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Description

BD 309680 – TRAY CONVENIENCE BULK STE

60 mL BD Luer-Lok Syringe Bulk Sterile Pharmacy Convenience Tray

 

BD sterile syringe convenience trays help pharmacy staff save time and effort when batch-preparing syringes.

CE Mark Product is CE-marked
Pyrogen Free Product is pyrogen free
Syringe Tip Orientation Concentric
Syringe Tip Type BD Luer-Lok
Syringe Scale 1 mL graduations
Sterility Sterile
Total Shelf Life 1825
Volumetric Accuracy +/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml
Sterilization Method Radiation
Latex Free Not made with natural rubber latex

BD Luer-Lok Syringe

Bring security to critical applications

The BD Luer-Lok 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 5-mL syringe’s scale has 1/5 mL graduation.

2018 03 08 14 27 39 BD PLASTIPAK 10ML HYPODERMIC SYRINGE STERILE LUER LOK 300912 eBay bniah9

BD Luer-Lok Tip

BD Luer-Lok tip is generally used for injections requiring a secure connection of the syringe to another device.


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 E-beam. Sterilization cycle development/validation is performed to 10-6SAL 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

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