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Part Number
Teleflex AK-14553
SKU Number
CIA2258370
Sell Unit
CASE
Ships Within
Call for Availability
List Price
$889.43
Product Description
Teleflex AK-14553 - Three-Lumen Central Venous Catheter (CVC) for Femoral Vein Insertion, 5.5 Fr X 30cm, 5/CS
Teleflex AK-14553 Three-Lumen Central Venous Catheter
Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter For Femoral Vein Insertion.
Teleflex AK-14553 Three-Lumen Central Venous Catheter Indications for Use
The Arrow catheter is indicated to permit short-term (< 30 day) central venous access for the treatment of diseases or conditions requiring central venous access, including, but not limited to the following:
- Lack of usable peripheral IV sites
- Central venous pressure monitoring
- Total parenteral nutrition (TPN)
- Infusions of fluids, medications, or chemotherapy
- Frequent blood sampling or receiving blood transfusions/blood products
Precautions of Teleflex AK-14553 Three-Lumen Central Venous Catheter
- Do not alter the catheter, guidewire or any other kit/set component during insertion, use or removal.
- Procedure must be performed by trained personnel well versed in anatomical landmarks, safe technique and potential complications.
- Use standard precautions and follow institutional policies for all procedures including safe disposal of devices.
- Some disinfectants used at catheter insertion site contain solvents which can weaken the catheter material. Alcohol, acetone, and polyethylene glycol can weaken the structure of polyurethane materials. These agents may also weaken the adhesive bond between catheter stabilization device and skin.
- Ensure catheter patency prior to use. Do not use syringes smaller than 10 mL (a fluid filled 1 mL syringe can exceed 300 psi) to reduce risk of intraluminal leakage or catheter rupture.
- Minimize catheter manipulation throughout procedure to maintain proper catheter tip position.
Device Characteristics of Teleflex AK-14553 Three-Lumen Central Venous Catheter
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": | Yes |
For Single-Use: | Yes |
Prescription Use (Rx): | Yes |
Over the Counter (OTC): | No |
Kit: | Yes |
Combination Product: | Yes |
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P): | No |