Moog Medical 340-4172 - MICROBORE TUBING W/ VENTED 0.22 FILTER, ANTI-SIPHON VALVE, 20 PER/CS
Ambulatory Pump Sets with IN-Line Anti-Siphon Valves (ASV)
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.
- Do not contain DEHP or rubber tree latex.
340-4172 - 86 / 3.6 mL Non-DEHP Microbore Tubing with Vented 0.2 Micron Filter and 150ml Medication Reservoir with Individually Packaged Non-Vented Male/Female Luer Lock Cap
150 mL medication reservoir, microbore tubing with free-flow protection, slide clamp, ASV 6 inches from distal end, male luer lock connector. Non-vented male/female luer lock cap packaged separately. Priming volume: 3.7 mL, Length: 92 in. (233.7 cm)
- Common Usage: Small Volume Requiring 0.2 Micron Filter
- Length/Fill Volume: 86 / 3.6 mL
- Position of In-Line ASV: 6" from the distal end
- Non-ASV Set Equivalent: 340-4119
- 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.
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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 |
Moog Medical #340-4174, NON-DEHP TUBING W/ VENTED BAG SPIKE AND 0.22 FILTER, ANTI-SIPHON VALVE, 20 PER/CS
Moog Medical #340-4119, MICROBORE TUBING W/ VENTED 0.22 FILTER, W/ 150ML ME, 20 PER/CS
Moog Medical #340-4171, EPIDURAL YELLOW STRIPED TUBING, 0.22 FILTER, W/ ANTI-SIPHON VALVE, 20 PER/CS
