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BD 309695 Syringe Control 10cc L/L Tip Sterile 100/CS

As demand for our products continues to rise, our inventory levels are changing rapidly on a daily basis. If you need your order shipped immediately, please contact us as soon as possible so we can ensure that your order is fulfilled in a timely manner.

Orders@healthsupply770.com
Phone: 850-708-4904

$149.99

BD 309695 Syringe Control 10cc L/L Tip Sterile 100/CS

309695 – 10 mL BD Control Syringe with BD Luer-Lok tip sterile

  • Luer-Lok Tip
  • Latex Free
  • Not for Oral use
  • Do not reshield used needles
  • Dsicard after single use
  • Sterile
  • Single use

BD Luer-Lok tip

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

Great For

  • Irrigation
  • Hydroponics
  • Giving medicine like cough syrup to kids
  • First Aid
  • Jello or Alcohol Shots

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
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.

Sterilization cycle development/validation is performed to 10-6 SAL in accordance with current ISO 11137 guidelines.

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 Case Each Shelfpack
Quantity 100 1 25
Length 418.0 mm 280.0 mm
Width 280.0 mm 200.0 mm
Height 280.0 mm 178 mm
Weight 3.18 kg 31.8 g 795.0 g