ISO 18250-3 First edition 2018-06

Medical Devices - Connectors For Reservoir Delivery Systems For Healthcare Applications - Part 3: Enteral Application

18250-3 First edition 2018-06

Standard Organization: ISO

ISO 18250-3 First edition 2018-06
Medical devices - Connectors for reservoir delivery systems for healthcare applications - Part 3: Enteral application

Recognition NumberGeneral I (QS/RM)
Recognition Date2018-09-17
Recognition List050
Recognition Number5-119
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

Rationale:

This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies.

Scope:

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.

Code of Federal Regulations:

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

FDA Guidance:

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


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