BD #303346 - Syringe w/ Plast Cannula 3cc 100/BX, 8 BX/CS

BD #303346 - Syringe w/ Plast Cannula 3cc 100/BX, 8 BX/CS
CIA1009603
BOX
24 Hours
$42.45

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Product Description

BD Part #303346 - Syringe w/ Plast Cannula 3cc 100/BX, 8 BX/CS

Syringes with BD Cannula for use with Baxter Interlink, Abbott LifeShield, or B. Braun SafeLine Systems

303346 - 3 mL Syringe with BD Blunt Plastic Cannula (syringe cannula)

The BD blunt plastic cannula is a truly universal cannula designed to be used with all types of split septum IV injection sites and vials for needleless access.

Compatibility

The cannula and accessories are compatible with BD VersaSafe, Abbott LifeShield, B. Braun Safeline and Baxter Interlink IV access systems.


Key Product Features

SterileSterilized product
Safety EngineeredSafety engineered product
Safety Engineered FeatureNeedleless
Sterilization MethodGamma irradiation
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 E-beam. Sterilization cycle development/validation is performed to 10-6 SAL 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.

Biocompatability

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

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 LevelShelfpackEachCase
Quantity1001800
Length210.0 mm419.0 mm
Width188 mm381.0 mm
Height170 mm330.0 mm
Weight620.0 g5.2 g5.375 kg