BD 302832 Syringe 30cc LL 224/CS

$129.00

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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
Brand BD
CE Mark Product is CE-marked
Parenteral Parenteral product
Pyrogen Free Product is pyrogen free
Syringe Tip Type BD Luer-Lok
Sterilization Method Irradiation
Application General Purpose Syringe
Color Translucent Barrel / Black Markings / Translucent Plunger
Graduations 1 mL Increments
Safety Feature Without Safety
Sterility Sterile
Material Plastic
Style Flat Top
Tip Type Luer Lock Tip
Volume 30 mL
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.

CE-marked

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.

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 10-6SAL 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

Sterilization

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

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