AMT ENFit Transition Adapter

AMT ENFit is a patient safety initiative designed to ensure that feeding tube connectors are incompatible with connectors used for unrelated delivery systems, such as trach tubes, IV lines, and catheters. The enteral transition adapters are available in several configurations, each offering different connection options for enteral devices currently on the market.

Features

• Single user use.
• Material: DEHP.
• Non-sterile.
• Latex-free.
• TRN101: Male Enfit to Male Luer
• TRN201: Female Enfit to Female Luer

Indications For Use

The AMT Enteral Transition Adapters are intended to facilitate enteral-specific connections between AAMI/CN3(PS) compliant connectors and non ISO 80369-1 compliant legacy enteral connectors.

Contraindications

At this time, there are no contraindications for the use of the ENFit Transition Adapters.

Complications

At this time, there are no complications associated with the use of the ENFit Transition Adapters.

Clinical Benefits

Clinical benefits to be expected when using the ENFit Transition Adapters include, but are not limited to: Provides a connection method between feeding sets, extension sets, and syringes with ENFit connectors and enteral connections with non-ENFit compliant connecting ends.

Performance Characteristics

Performance characteristics of the ENFit Transition Adapters include, but are not limited to: providing connections between giving sets and syringes with ISO 80369-3 ENFit connectors and enteral connections with non-ISO 80369-3 compliant connecting ends.

• Wide variety of ENFit Transition Adapters
• Forward and backwards compatibility - the ability to connect the current market to ENFit and connect ENFit to the current market
• Glow Green Technology provides better visibility in the dark for easier nighttime feeds
• Easily removed for cleaning between uses

Device Longevity

Always remove the transition adapter from the legacy adapter after each use. The transition adapter is reusable. Depending on usage (frequency, environment, etc.), periodic replacement of the adapter may be necessary for optimal functionality. Replace the adapter if any leakage or cracks occur.

• The product warranty is applicable as per the terms and conditions provided by the product manufacturer.

Please call us for specific details.

• No returns will be accepted after 30 days from the date of shipment.
• All returns are subject to a restocking fee as per manufacturers terms and conditions.
• All returns must have an RGA number (Returned Goods Authorization), unauthorized returns will not be accepted.
• We do not guarantee fulfillment of any desired purpose or product suitability to the user and this will not be considered as a valid reason for return.
• The products must be new, unused condition, not tampered with, in original packaging and returned at the customers expense in the original packaging.
• If your return is not due to any manufacturing defect then the original shipping cost will be deducted from the total refund.
• Hygiene, bath and toilet items cannot be returned once opened or used.
• Standard manufacturer terms and conditions apply for return policy of this product.

Please call us for specific details.

What is ENFit ?

The International Organization for Standardization (ISO) has established a standardized design for enteral connectors known as the “ENFit Connector.” These connectors are intended to improve patient safety by reducing the risk of medical device misconnections. ENFit connectors are intentionally designed to be incompatible with Luer adapters commonly used in IV applications. While similar in appearance to a threaded lock system, ENFit connectors are larger in size and therefore incompatible with Luer connections. ENFit is a global patient safety initiative developed to ensure enteral feeding connectors are not compatible with connectors used for unrelated delivery systems such as tracheostomy tubes, IV lines, and catheters. Although misconnections are relatively uncommon, they can result in serious clinical consequences. The ENFit system was developed as part of the Stay Connected initiative with oversight from clinicians, manufacturers, and regulatory bodies.

What Does This Mean for You?

The primary change involves how the nutrition source connects to the feeding set, which then connects to the enteral feeding device. Straight and right-angle connectors that attach to low-profile feeding devices remain unchanged. The distal end of feed sets that connect directly to the device is not currently regulated under this standard.