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Moog Medical 340-4162 - EPIDURAL YELLOW STRIPED TUBING, 114IN, NON-VENTED SPIKE, 0.2U FILTER, 20 PER/CS

Moog Medical # 340-4162 - EPIDURAL YELLOW STRIPED TUBING, 114IN, NON-VENTED SPIKE, 0.2U FILTER, 20 PER/CS
Part Number Moog Medical 340-4162
SKU Number CIA7004422
Sell Unit CASE
Ships Within Special Order
List Price $286.19
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Product Description

Moog Medical 340-4162 - EPIDURAL YELLOW STRIPED TUBING, 114IN, NON-VENTED SPIKE, 0.2U FILTER, 20 PER/CS

340-4162 - 114" / 3.8 mL Non-DEHP Epidural Yellow-Striped Tubing with Vented 0.2 Micron Filter

Non-vented bag spike, epidural yellow-striped tubing with free-flow protection, slide clamp, vented 0.2 micron filter. distal male luer lock connector. Priming volume: 4.5 mL, Length: 114 in. (290 cm)

All administration sets designed for use with Moog's Curlin line of infusion pumps include anti-free flow feature that prevents inadvertent free flow of the infusion. This unique and patented anti-free flow device also allows the intentional priming of the set by gravity, thereby reducing the set-up time. In addition to the standard administration sets, Moog features administration sets with an anti-siphon valve included for additional anti free-flow protection All ambulatory infusion administration sets can be used with the Moog 6000 CMS, PainSmart IOD, and 4000 CMS electronic infusion pumps.

  • Wash your hands thoroughly.
  • Remove the administration set (tubing) from the package.
  • Twist off the break-away tab located on the bottom of the yellow Flow-Stop (see diagram below).
  • Follow your clinicians instructions for inserting the bag spike into the IV bag so that it is not contaminated.
  • If a Back Check Valve Adapter is provided with your administration set, remove it from the package and connect it to the end of the tubing.

Preparing Medication for Infusion/Changing IV Bags

Spiking the fluid container, gravity priming the set and using the slide clamp to close the tubing.

Curlin Medical Administration set "Integral Flow-Stop" with breakaway tab

Intentionally Opening the "Integral Flow-Stop"

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