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BD 302832 - Syringe 30cc LL 56/Bx, 4 BX/CA
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
- 30 ml capacity
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
|CE Mark||Product is CE-marked|
|Pyrogen Free||Product is pyrogen free|
|Syringe Tip Type||BD Luer-Lok|
|Application||General Purpose Syringe|
|Color||Translucent Barrel / Black Markings / Translucent Plunger|
|Graduations||1 mL Increments|
|Safety Feature||Without Safety|
|Tip Type||Luer Lock Tip|
|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|
|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.
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.
|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|
|Prescription Use (Rx)||Yes|
|Over the Counter (OTC)||No|
|Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)||No|
|Device Packaged as Sterile:||Yes|
|Requires Sterilization Prior to Use:||No|