Avanos Medical 20-9368 - CORFLO Nasogastric/Nasointestial Feeding Tube with Stylet, 10 EA/CS

Part Number Avanos Medical 20-9368

SKU Number CIA7005917

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Product Description

Avanos Medical 20-9368 - CORFLO Nasogastric/Nasointestial Feeding Tube with Stylet, 10 EA/CS

AVANOS CORFLO Nasogastric/Nasointestinal Feeding Tube with Stylet is uniquely designed for delivering enteral nutrition. Each package comes with a variety of features that provide consistent performance and convenience, including an anti-clog bolus, centimeter markings, and a water activated lubricated tip and internal lumen.Multiple Choices for Clinician Convenience With multiple packages from which to choose, clinicians can choose whether or not they want ENFit, Universal, and Anti-IV proximal connectors. Similarly, Avanos polyurethane CORFLO NG/NI tubes are available in various lengths and French sizes. Avanos Medical, a leader in the enteral feeding market, offers a wide variety of innovative, high-quality enteral feeding tubes and accessories designed for delivering enteral nutrition.

The AVANOS CORFLO Nasogastric/Nasointestinal Feeding Tube is a medical grade polyurethane feeding tube that has been specifically designed for patient comfort and safety during tube insertion and use. It is intended for use in patients who require intermittent or continuous tube feedings via the nasogastric or nasointestinal pathway. Options include sterile/non-sterile, weighted/non-weighted, and with/without stylet.

Avanos 20-9368 CORFLO Nasogastric/Nasointestinal Feeding Tube With Stylet Features

Weighted/Non-Weighted
With and without stylet
ENFit, Universal, and Anti-IV proximal connectors
Anti-clog bolus
CM Markings
MRI conditional once stylet is removed
Flow-Through Stylet
Radiopaque
Water Activated Lubricated Tip & Internal Lumen (stylet tubes only)

The Avanos CORFLO NG/NI feeding tubes are available in a wide variety of adult, pediatric and neonatal sizes. Their polyurethane construction makes them excellent for long-term intubation and offers a larger lumen than PVC tubes and Silicone tubes of the same French size.

Designed to prevent feeding tube misconnections, CORFLO NG/NI feeding tubes with ENFit connectors feature a clear connector housing for visual inspection of connection with administration sets, as well the inspection of cleanliness before, during and after use. In line with National Patient Safety Agency guidance CORFLO NG/NI tubes are fully radiopaque along their entire length, are CE marked and have external visual length markings.

Avanos 20-9368 CORFLO Nasogastric/Nasointestinal Feeding Tube

Indications for Use

The AVANOS CORFLO Feeding Tube is intended for use in those patients who require intermittent or continuous tube feedings via the nasogastric or nasoenteric route.

Tube Insertion

This feeding tube is to be inserted by trained and competent individuals or clinicians, following institution/facility/hospital protocols.

Explain procedure to patient if applicable.
2. Position patient in sitting or Fowlers position as tolerated.
Warning: The patient should not lean forward, nor should the head and neck be extended.
Caution: Do not use a stylet if the tube is not packaged with one, as the stylet may exit the distal tip.
Remove tube from package. Close access ports.
Measure length of tube to be inserted to ensure that tip/bolus enters the gastric region. Place exit port of tube at tip of nose. Extend tube to earlobe, then to xiphoid process (Fig 8). Use the printed centimeter marks on the tube to aid intubation and check for tube migration.
Warning: Premeasurement of tubing length is essential.
Do not insert excess. Occlusion may result from kinking of tube.
Determine preferred nostril for insertion. Provide cooperativepatient with glass of water and straw.
Prior to insertion, activate lubricant on tip by dipping in water.
Direct tube posteriorly, aiming tip parallel to nasal septum and superior surface of hard palate. Advance tube to nasopharynx, allowing tip to seek its own passage. As patient swallows sips of water, advance tube through esophagus into stomach with gentle motion.
Utilize printed centimeter marks on the tubes to aid insertion.
Confirm tube position and integrity per institution/facility/hospital protocol (e.g. pH measurement, X-ray, etc.).
For tubes packaged with a stylet: After tube position in the stomach is confirmed, remove stylet by flushing tube through the side port with up to 10 ml of water to activate internal lubricant immediately prior to stylet removal.
Secure tube per institution protocol.

Tube Maintenance

Follow your institution/facility/hospital protocol or clinicians order.
It is recommended the tube be irrigated every 4 hours with up to 20 ml of water (up to 10 ml for infants or children) before and after medication administration or when feeding formula is interrupted.
Warning: Vigorous syringe force should not be used to irrigate, administer liquids or unblock the tube.
The feeding tube should be monitored, regularly assessed, and replaced when clinically indicated based on functionality and patient condition.

AVANOS CORFLO Nasogastric / Nasointestinal Feeding Tubes

Tube Capped (Fig. 6)

Feed Port
Auxiliary Port

Tube Connected (Fig. 7)

Administration Set
Syringe

Features:

Distinctive YELLOW tube design
Exit ports:
Anti-clog bolus
Bolus
ENFit design employed for reducing the risk of tubing misconnections. ENFit satisfies the ISO Standard (80369-3) for small bore enteral devices.
Water-activated C-19 lubricant on tube tip
Dual port to maintain closed system
For YELLOW feeding tubes Radiopacity: 20% barium tube, 40% barium tip

Ability to Connect to Non-Enteral Medical Devices

The ENFit connectors were designed to prevent misconnections between enteral devices and other devices used in various medical applications. However, the design of the ENFit connector cannot overcome all chances of misconnection. The following connector types are potential misconnections for the ENFit connector (feeding/ medication access port) of this enteral feeding tube:

Suction ports on Endotracheal Suction Systems
Respiratory circuit filtration connectors
Oxygen inlet connectors for Resuscitation Devices
Baxter IV Solution Bag ports (such as NaCl, Ringers Solution, etc.)
Sample ports on drainage bags
Peritoneal Dialysis connectors
Cones & sockets of ISO 5356-1:2004 & ISO 5356-2:2004
Temperature sensor connectors & mating ports of ISO 8185:2007
Oxygen nipples as defined in EN 13544-2:2002

CORFLO NG/NI feeding tubes have satisfied biocompatibility testing as a device for long-term use per ISO 10993-1.

Avanos 20-9368 CORFLO Nasogastric/Nasointestinal Feeding Tube MRI Safety Information

Non-clinical testing demonstrated that the weighted CORFLO Enteral Feeding Tubes are MR Conditional. A patient with this device can be scanned safely immediately after placement under the following conditions:

Static magnetic field of 3-Tesla or less
Spatial gradient magnetic field of 720-Gauss/cm or less
MR system reported whole body averaged SAR of 3.0-W/kg

(i.e., associated with a calorimetry measured value of 2.8- W/kg) Under the conditions described above using a transmit/receive RF body coil the CORFLO Enteral Feeding Tube produced the highest temperature change of +1.5 ?C during MRI performed for 15-min in the 3-Tesla (3-Tesla/ 128-MHz, Excite, Software G3.0-052B, General Electric Healthcare, Milwaukee, WI) MR system.

Artifact Information: MR image quality may be compromised if the area of interest is relatively close to the position of the CORFLO Enteral Feeding Tube. Therefore, optimization of MR imaging parameters to compensate for the presence of this device may be necessary.

Avanos 20-9368 CORFLO NasogastricNasointestinal Feeding Tube With Stylet With Enfit Connector MRI

Avanos CORFLO Nasogastric/Nasointestinal Feeding Tube 20-9368 Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No