ISO 18250-3 First edition 2018-06 Medical devices - Connectors for reservoir delivery systems for healthcare applications - Part 3: Enteral application |
Recognition Number | General I (QS/RM) |
Recognition Date | 2018-09-17 |
Recognition List | 050 |
Recognition Number | 5-119 |
Extent | Complete standard |
Standards Orgs | ISO International Organization for Standardization https://www.iso.org/ |
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FDA Tech | Mark Antonino FDA/OMPT/CDRH/ODE/DRGUD/GEDB/ 240-402-9980 Mark.Antonino@fda.hhs.gov |
This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies.
This document specifies dimensions and requirements for the design and functional performance of connectors intended to be used on enteral reservoirs.
This document does not specify the dimensions and requirements for the medical devices or accessories that use these connectors. Such requirements are given in particular International Standards for specific medical devices or accessories.
Regulation Number | Device Name | Device Class | Product Code |
§876.5980 | Enteral Specific Transition Connectors | Class 2 | PIO |
§876.5980 | Enteral Syringes With Enteral Specific Connectors | Class 2 | PNR |
§876.5980 | Gastrointestinal Tubes With Enteral Specific Connectors | Class 2 | PIF |
§876.5980 | Set, Gavage, Infant, Sterile | Class 2 | FHT |
§876.5980 | String And Tubes, Gastrointestinal, To Locate Internal Bleeding | Class 2 | FFW |
§876.5980 | Tube, Feeding | Class 2 | FPD |
§876.5980 | Tube, Gastro-Enterostomy | Class 2 | KGC |
§876.5980 | Tube, Nasogastric | Class 2 | BSS |
§876.5980 | Tube, Single Lumen, With Mercury Wt Balloon For Intestinal Intubation And / Or Decompression | Class 2 | FEF |
§876.5980 | Tubes, Gastrointestinal (And Accessories) | Class 2 | KNT |
Guidance for Industry and Food and Drug Administration Staff: Safety Considerations for 510(k) Submissions to Mitigate the Risks of Misconnections with Small-bore Connectors Intended for Enteral Applications, Issued February 11, 2015. (Website) Information for Manufacturers of Small-Bore Connectors and Medical Devices with Connectors http://www.fda.gov/medicaldevices/safety/alertsandnotices/tubingandluermisconnections/ucm313322.htm |