BD 303347 Syringe 5cc Interlink System IV Blunt Cannula w/oNdl 17 Gauge 400/CS

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BD 303347 Syringe 5cc Interlink System IV Blunt Cannula w/oNdl 17 Gauge 400/CS

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

303347 – 5 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.


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

Key Product Features

Sterile Sterilized product
Safety Engineered Safety engineered product
Safety Engineered Feature Needleless
Sterilization Method Gamma irradiation
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.


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.


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.


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-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

Product Packaging Information

Packaging Level Shelfpack Each Case
Quantity 100 1 400
Length 280.0 mm 419.0 mm
Width 210 mm 280.0 mm
Height 192 mm 375.0 mm
Weight 940.0 g 9.7 g 3.88 kg