In Stock


BD 302832 Syringe 30cc LL 224/CS

Product Description:

BD 302832 Syringe 30cc LL 224/CS

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

30 mL BD Syringe Only

30mL Luer-Lok tip syringe, disposable. No needle. BD syringes feature a clear barrel with bold scale markings, tapered plunger rod for ease of aspiration, positive plunger rod stop, and an added BD Luer-Lok thread for increased secure connection.

  • Luer-Lok Tip
  • Latex Free
  • Sterile if Package Intact
  • Non-Pyrogenic
  • 30 ml capacity
2018 03 08 14 27 39 BD PLASTIPAK 10ML HYPODERMIC SYRINGE STERILE LUER LOK 300912 eBay bniah9

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

Manufacturer No.302832
CE MarkProduct is CE-marked
ParenteralParenteral product
Pyrogen FreeProduct is pyrogen free
Syringe Tip TypeBD Luer-Lok
Sterilization MethodIrradiation
ApplicationGeneral Purpose Syringe
ColorTranslucent Barrel / Black Markings / Translucent Plunger
Graduations1 mL Increments
Safety FeatureWithout Safety
StyleFlat Top
Tip TypeLuer Lock Tip
Volume30 mL
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.


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.

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


Device Packaged as Sterile:Yes
Requires Sterilization Prior to Use:No