BD #309657 - Syringe 3cc LL w/o Needle Shelf Pack 200/Bx, 4 BX/CA

BD #309657 - Syringe 3cc LL w/o Needle Shelf Pack 200/Bx, 4 BX/CA
CIA1119361
CASE
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$72.44

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Product Description

BD Part #309657 - Syringe 3cc LL w/o Needle Shelf Pack 200/Bx, 4 BX/CA

BD Luer-Lok Syringe

309657 - 3 mL BD Luer-Lok Syringe Sterile, Single use

  • Sterile
  • Do Not Reuse
  • Do Not Reshield Used Needles
  • Not made with natural rubber latex
  • Not made with DEHP

BD Luer-Lok Tip

Bring Security to Critical Applications

  • BD Luer-Lok thread: The BD Luer-Lok thread provides a secure connection.
  • Plunger rod design: Each disposable syringe features a tapered plunger rod for ease of aspiration and a positive plunger rod stop.
  • Ease of use: BD syringes feature a clear barrel with bold scale markings.

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,EO
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.

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.

This product is primarily sterilized via Gamma. Sterilization cycle development/validation is performed to 10-6 SAL in accordance with current ISO 11137 guidelines.

Biocompatability

This product has been evaluated in accordance with ISO 10993 "Biological Evaluation of Medical Devices", and complies with all relevant sections.

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

Product Packaging Information

Packaging LevelShelfpackCaseEach
Quantity2008001
Length30.0 cm30.0 cm
Width19.0 cm38.0 cm
Height17.3 cm34.6 cm
Weight1.034 kg4.136 kg5.17 g