Dynarex 3-Port Gastrostomy Tube with ENFit® Connector, 12–24 Fr, Silicone, Sterile, CS/5EA – Select Size
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Product Details
Dynarex 3-Port Gastrostomy Tube with ENFit® Connector, 12–24 Fr, Silicone, Sterile, CS/5EA – Select Size is designed for enteral feeding and medication administration across hospital, long-term care, and home-care environments. Its sterile silicone construction features a double-lumen shaft with proximal ENFit® safety access ports, an external retention disk, balloon, and distal open flow-through tip.
The three-port design helps support caregiver access while the ENFit® connection is designed to reduce the risk of enteral misconnections. Available in seven French-size options from 12 Fr through 24 Fr and sold in cases of five.
Key Features
| Enteral Feeding Design | Patient & Caregiver Features | Product Configuration |
|---|---|---|
| Three-port gastrostomy tube | ENFit® safety connector | Sterile silicone |
| Designed for enteral nutrition | Rounded distal tip | 12–24 Fr sizes |
| Supports medication administration | External retention disk | 7 selectable sizes |
| Double-lumen shaft | Balloon retention | 5 tubes per case |
| Distal open flow-through tip | Color-coded size configuration | Rx-only medical device |
Shared Specifications
| Attribute | Details | Attribute | Details |
|---|---|---|---|
| Brand | Dynarex | Manufacturer | Dynarex Corporation |
| Product Type | 3-Port Gastrostomy Tube | Connector | ENFit® |
| Size Range | 12–24 Fr | Number of Variants | 7 |
| Material | Silicone | Sterility | Sterile |
| Number of Ports | 3 | Shaft Configuration | Double Lumen |
| External Retention | Retention Disk | Internal Retention | Balloon |
| Distal Tip | Rounded / Open Flow-Through | Application | Enteral Feeding / Medication Administration |
| ENFit® Safety Ports | Yes | Rx Only | Yes |
| Natural Rubber Latex | Not Made with Natural Rubber Latex | BPA | Not Made with BPA |
| Phthalate Plasticizers | Not Made with Phthalate Plasticizers | DEHP | Free |
| HCPCS | B4087 | UNSPSC | 42231601 |
| Country of Origin | Israel | Minimum Selling Unit | CS |
| Packaging | CS/5EA | Authorized EA Sales | No |
Dynarex identifies the family as silicone, sterile, Rx-only, DEHP-free, not made with natural rubber latex, and HCPCS B4087.
Variant-Specific Specifications
| Tube Size | MPN | Approx. Outside Diameter | Color Identification |
|---|---|---|---|
| 12 Fr | 5111 | 4.0 mm | White |
| 14 Fr | 5112 | 4.7 mm | Green |
| 16 Fr | 5113 | 5.3 mm | Orange |
| 18 Fr | 5114 | 6.0 mm | Red |
| 20 Fr | 5115 | 6.7 mm | Yellow |
| 22 Fr | 5116 | 7.3 mm | Violet |
| 24 Fr | 5117 | 8.0 mm | Blue |
Dynarex’s current individual product records confirm the size-specific outside diameters and color identification shown above.
Warnings
| Professional Use | Placement & Feeding | Sterility & Device Safety |
|---|---|---|
| Prescription-use medical device | Select the appropriate French size for the patient | Do not use if sterile packaging is damaged |
| Intended for appropriately trained healthcare professionals and caregivers | Confirm proper tube placement before feeding or medication administration | Single-use device |
| Follow current manufacturer instructions for insertion and replacement | Inflate and manage the retention balloon according to manufacturer instructions | Do not reuse or resterilize |
| Use ENFit®-compatible enteral equipment | Monitor tube position and gastrostomy site | Inspect tubing, ports, disk, and balloon before use |
| Flush according to prescribed enteral-care protocols | Do not force incompatible connectors into ENFit® ports | Verify expiration dating before use |
| Follow prescribed enteral nutrition and medication protocols | Maintain appropriate external retention-disk positioning | Dispose of according to applicable facility procedures |
Specifications
- SterilitySterile
- Single PatientYes
- Autoclave ReadyNo
