Avanos ENFit® Enteral Distal-End Transition Connector, NonSterile, (CS/200EA)
Avanos ENFit® Enteral Distal-End Transition Connector provides a secure transition between compatible ENFit and legacy enteral feeding components. Designed for enteral feeding systems, the single-use connector is nonsterile and available in PK/5EA or CS/200EA.
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Product Details
Avanos ENFit® Enteral Distal-End Transition Connector, NonSterile, PK/5EA & CS/200EA is a specialized feeding-tube accessory designed to support transitions between ENFit® and non-ENFit enteral feeding components.
The connector is intended for use with enteral feeding systems and provides a dedicated enteral connection pathway during equipment transitions. Avanos identifies the product as a nonsterile, prescription-use Feeding Tube Accessory, while FDA AccessGUDID lists it as an ENFit/non-ISO 80369 standardized linear connector in current commercial distribution.
Key Features
| Enteral Compatibility | Product Design | Packaging |
|---|---|---|
| Designed for enteral feeding systems | Distal-end transition connector | 5 connectors per pack |
| ENFit® transition functionality | Single-use | 40 packs per case |
| Supports equipment transition | NonSterile | 200 connectors per case |
| Feeding-tube accessory | Prescription use | PK and CS selling units |
| Dedicated enteral connector | Not made with natural rubber latex | Compact lightweight packaging |
Specifications
| Attribute | Details | Attribute | Details |
|---|---|---|---|
| Brand | Avanos | Manufacturer | Avanos Medical |
| MPN | 7149-00 | McKesson Item # | 1105103 |
| Product Name | Enteral Distal-End ENFit® Transition Connector | Application | Transition Connector |
| Product Type | Feeding Tube Accessory | For Use With | Enteral Feeding Sets |
| ENFit | Yes | Sterility | NonSterile |
| Usage | Single Use | Prescription Use | Yes |
| FDA Product Code | PIO | FDA Device Class | Class II |
| Primary DI / GTIN | 08056093720716 | Pack DI | 08056093720723 |
| Case Package DI | 08056093720730 | Natural Rubber Latex | Not Made with Natural Rubber Latex |
| HCPCS | B4036 – verify payer-specific billing | UNSPSC | 42231505 |
| BAA Compliant | No | TAA Compliant | No |
| Country of Origin | Unknown | Minimum Sellable Units | PK; CS |
| PK Packaging | 5 EA/PK | CS Packaging | 40 PK / 200 EA |
McKesson confirms MPN, application, HCPCS B4036, UNSPSC, BAA/TAA status, and packaging. FDA AccessGUDID confirms the device identifiers, Class II enteral-transition-connector classification, single-use status, Rx designation, nonsterile status, and latex labeling.
Packaging Identifiers
| Packaging Level | Quantity | Device Identifier |
|---|---|---|
| Individual Device | 1 EA | 08056093720716 |
| Pack | 5 EA | 08056093720723 |
| Case Level | 40 PK = 200 EA | 08056093720730 |
FDA AccessGUDID currently lists these package identifiers in commercial distribution.
Warnings
| Enteral Use | Connection Safety | Handling |
|---|---|---|
| For enteral applications only | Verify correct ENFit compatibility before connection | Single-use device |
| Do not connect to incompatible systems | Ensure connection is secure before feeding | NonSterile |
| Follow the feeding-system manufacturer's instructions | Never force mismatched connections | Do not reuse |
| Verify the complete feeding pathway before administration | Use only with appropriate enteral equipment | Inspect packaging/device before use |
| Prescription-use product | Follow facility enteral-feeding protocols | Dispose according to facility policy |
Specifications
- SterilitySterile
- Single PatientYes
- Autoclave ReadyNo
