BD 302833 Syringe Only Slip-Tip 30cc 224/CS

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Description

BD 302833 Syringe Only Slip-Tip 30cc 224/CS

302833- 30 mL BD Luer Slip Tip Syringe sterile, Single use

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. Packaging is clearly labeled latex free.

  • For Diabetic and other uses including Post-Operative Conditions, Vitamin Deficiencies and Intramuscular Medication
  • Syringe Only
  • 30ml
  • Luer Slip Tip
  • Color Translucent Barrel / Black Markings / Translucent Plunger
  • 56 per box / 4 boxes per case
2018 03 08 14 27 39 BD PLASTIPAK 10ML HYPODERMIC SYRINGE STERILE LUER LOK 300912

Luer Slip Tip

Our luer slip tip provides a friction-fit connection that requires you to push and twist the syringe tip into the needle hub.

Key Product Features

CE Mark Product is CE-marked
Parenteral Parenteral product
Pyrogen Free Product is pyrogen free
Syringe Tip Type BD Luer Slip Tip
Syringe Scale 1 mL graduations
Sterile Sterilized product
Sterilization Method 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.

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 10-6 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.

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

Cautions

  • To help avoid HIV (AIDS), HBV (Hepatitis) and other infectious disease due to accidental needlesticks, used needles should not be recapped or removed, unless there is no alternative or such action is required by a specific medical procedure. OSHA (USA) standards require that recapping of needles must performed using a one handed technique
  • Federal (USA) law restricts this device to sale by or on the order of a physician.
  • Re-use may lead to infection or other illness/injury.

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