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Part Number
Teleflex HO-14703
SKU Number
CIA2042664
Sell Unit
CASE
Ships Within
24 Hours
List Price
$413.99
Product Description
Teleflex HO-14703 - HANDS-OFF Three-Lumen Central Venous Catheter for use only with Arrow One-Piece PSI System, 7 FR X 30 CM, 5/CS
Teleflex HO-14703 HANDS-OFF Three-Lumen Central Venous Catheter
HANDS-OFF(R) Multi-Lumen Central Venous Catheter with Blue FlexTip(R) for use only with Arrow One-Piece Percutaneous Sheath Introducer System
Teleflex HO-14703 HANDS-OFF Three-Lumen Central Venous Catheter Indications for Use
The central venous catheter permits venous access to the central circulation through an indwelling Arrow percutaneous sheath introducer.
Precautions of Teleflex HO-14703 HANDS-OFF 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.
- For blood sampling, temporarily shut off remaining port(s), if applicable, through which solutions are being infused.
Device Characteristics of Teleflex HO-14703 HANDS-OFF 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: | No |
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P): | No |