BD 305210 - Oral Syringe 3mL Amber Color with Tip Cap, 500/CS
3 mL BD Amber Oral Syringe with non Luer tip
BD offers a broad range of syringes and accessories for safe, rapid, oral medication administration. Syringes feature easy-to-read scale markings for accuracy. They're designed to reduce the risk of medication dosing or administrative error, while meeting patient needs for all ages. Specific oral scale in milliliters and teaspoons. Amber syringes meet USP requirements for photo-sensitive medications. Safe and effective administration of oral medication. DNR (Latex) free. Non sterile.
- Safe and effective administration of oral medication
- Specific oral scale in milliliters and teaspoons
- Amber syringes meet USP requirements for photo-sensitive medications
- Feature easy-to-read scale markings for accuracy
- Designed to reduce the risk of medication dosing or administrative error, while meeting patient needs for all ages
Key Product Features
|CE Mark||Product is CE-marked|
|Syringe Tip Orientation||Oral|
|Syringe Tip Type||Oral tip|
|Syringe Scale||0.1 ml graduations|
|Volumetric Accuracy||+/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml|
|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.
|Device Packaged as Sterile:||Yes|
|Requires Sterilization Prior to Use:||No|
|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|