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ENFit US Conversion Progress

Updated: Feb 23

Based on GEDSA's recent member reports, top-rated hospitals (Among U.S. News & World Report’s Best Ranked U.S. Hospitals) are leading patient safety by establishing ENFit as the best practice. ( sources from GEDSA)


 


 


 

Conversion to enteral products (e.g., feeding tubes, connectors/adapters, syringes) with ENFit® connectors According to GEDSA's recent reports, most of the leading manufacturers (Including KB Medical Group Inc ) of enteral feeding administration sets that contain ENFit® Transition Connectors will stop providing the transition connectors with the sets starting in July 2022. These transition connectors allow enteral products with a female ENFit® connector to attach to legacy ( older style) enteral feeding tubes with a female opening (see the Attachment). The production of legacy enteral products is expected to decline coinciding with this change. Therefore, facilities that have not made the complete transition to enteral products having EN Fit® connectors must transition to safer products per this Patient Safety Advisory.




 

Benefits of ISO Standardization to the ENFit® Enteral Feeding Connector. ( sources from GEDSA)


 

ENFit™ SYRINGE 5ML WITHOUT CAP (480 Pcs)


  • LATEX FREE

  • DEHP FREE

  • EO STERILE

  • MATERIAL: PP



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