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BD 309695 - Syringe 10cc LL Tip Control 25/Bx, 4 BX/CA

BD  # 309695 - Syringe 10cc LL Tip Control 25/Bx, 4 BX/CA
Part Number BD 309695
SKU Number CIA1119363
Sell Unit CASE
Ships Within Call for Availability
List Price $779.70
Product Description

BD 309695 - Syringe 10cc LL Tip Control 25/Bx, 4 BX/CA

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

ParenteralParenteral product
Pyrogen FreeProduct is pyrogen free
Syringe Tip OrientationConcentric
Syringe Tip TypeBD Luer-Lok
Syringe Scale0.2 mL graduations
Total Shelf Life1825
SterileSterilized product
Volumetric Accuracy+/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml
Sterilization MethodRadiation
BPA FreeNot made with BPA
DEHP FreeNot made with DEHP
Latex StatementNot made with natural rubber latex
PVC FreeNot made with PVC
DisposableDisposable product
Single UseProduct 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.

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


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-UseYes
Prescription Use (Rx)Yes
Over the Counter (OTC)No
Combination ProductNo
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)No

Product Packaging Information

Packaging LevelCaseEachShelfpack
Length418.0 mm280.0 mm
Width280.0 mm200.0 mm
Height280.0 mm178 mm
Weight3.18 kg31.8 g795.0 g
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