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AMedP-1.15
Manufacturers and suppliers of tracheal, thoracic drainage, intravenous, urinary, aspiration and nasogastric tubing and connectors, and the multinational medical teams in NATO evacuation chains who depend on them being interchangeable
AMedP-1.15 is the NATO standard for connector interfaces on medical tubing used in the field - tracheal, thoracic drainage, intravenous, urinary, aspiration and nasogastric connectors - so equipment from different nations stays interchangeable.
AMedP-1.15 is the NATO Allied Medical Publication that standardises the connectors joining medical tubes, catheters and probes to the equipment they attach to in the field. It covers five connector families: tracheal tube connectors to respiratory apparatus, thoracic drainage tube connectors to collection systems, connectors used in intravenous transfusion, infusion and injection, and connectors for urinary, aspiration and nasogastric probes. The document's own concern is interoperability rather than clinical practice. It opens by explaining that "the use of similar medical products with incompatible connectors can cause problems when medical units from different countries take part in the evacuation of casualties," up to and including having to change a device that is already inserted into a patient. Chapter by chapter, it fixes which connector family serves which purpose and how the male and female ends of each are meant to fit together, so tubing and connecting equipment procured by different nations stays interchangeable in a multinational evacuation chain. It says nothing about how a device is tested, inspected or certified, and it carries no clinical or treatment content.
AMedP-1.15 is covered by STANAG 2178 in the catalogue - the NATO agreement by which nations commit to using it. AMedP-1.15 is the technical content; the STANAG is what gives it force, and a nation can ratify with reservations, as the document's own front matter provides for with a standing Record of Reservations. For an organisation, the practical route in is rarely the STANAG directly: it is a national or NATO contract or tender that names AMedP-1.15 or one of the connector families it covers. The document does not address "manufacturers" or "suppliers" by name the way some Allied Publications do; its own words speak to who needs the interoperability - "medical teams which participate in a multinational evacuation chain under NATO authority should have available compatible connections for medical tubes and catheters." In practice, meeting the connector geometry is work done by whoever designs or manufactures the tubes, catheters, probes and connecting equipment, since that geometry is what makes one nation's product fit another's.
cone fitting on the respiratory equipment, sized to the tube so gas flow is not restricted and accidental disconnection is minimised. Some tracheal tubes also carry an inflatable cuff whose inflation valve takes the small luer-type connector Chapter 5 covers.
flutter valve or a water-seal drainage system.
(Luer) connection used for vascular access, syringes and fluid or drug administration, and a threaded Luer Lock variant that resists the pressure that can build up during fluid transfer.
three-light configurations depending on whether they also carry a balloon-inflation line and an irrigation line; aspiration probe connectors colour-coded to the probe's size; nasogastric probe connectors matched to an enteral feeding system or a vacuum adaptor.
This page names what each family is for and how it is meant to fit together. The dimensions, thread forms, luer specifications, pressures and test methods that make each connector interchangeable are the document's own content and are not reproduced here.
Three points in AMedP-1.15 are easy to miss and matter more than the tables around them. First, on thoracic drainage: some small-caliber thoracic catheters use a luer-type female connector, and where that is unavoidable the document requires it to "be perfectly identified to avoid confusing it with an intravenous tube" - connecting a thoracic drain to an intravenous line, or the reverse, is exactly the error compatible-but-distinct connectors exist to prevent. Second, on Luer Lock connections: the document states this stronger, threaded connection "must not be used in cases in which patients are being moved," because its grip can transmit an abrupt pull straight to the catheter inserted in the patient rather than releasing at the connector - the opposite of what "Lock" suggests a safer choice would be. Third, on paediatric nasogastric probes: the document requires the connector to "not be compatible with the conic 6% male Luer connector to avoid at all times possible administration errors" - deliberate incompatibility, here, is the safety requirement rather than a defect.
Annex A names a set of civil ISO and EN connector standards without stating that meeting one satisfies another: ISO 80369-1 covers general requirements for small-bore connectors for liquids and gases in healthcare, and ISO 80369-7 covers the part specific to intravascular and hypodermic applications; ISO 5356-1 covers conical connectors for anaesthetic and respiratory equipment and ISO 5361 covers tracheal tubes and connectors specifically; ISO 16142-1 and ISO 16142-2 set essential principles of safety and performance for non-IVD and IVD medical devices respectively; and ISO 20697, ISO 20696, ISO 8836 and UNE-EN 1615 cover drainage catheters, urethral catheters, suction catheters and enteral feeding catheters and their connectors. None of these appears elsewhere in our catalogue as a linked record, so each is named plainly here.
AMedP-1.15 is an operational and technical NATO standard, not a management-system one, and its substance - choosing and building the right connector interface - is a hardware design and manufacturing decision, not something a compliance platform executes. Where ComplyTrain fits is the evidence trail around that decision: the design record showing which connector family and which referenced ISO or EN standard a product was built to; the record tying a colour-coding requirement or a deliberate compatibility exclusion, such as the paediatric nasogastric requirement, back to the clause that requires it; and the training record for staff who specify or select field medical tubing and connecting equipment.
What ComplyTrain does not do: it does not design, machine or dimensionally verify a connector, decide clinical procedure, or test a device against AMedP-1.15 or the ISO standards it points to. Which of AMedP-1.15, STANAG 2178 and the referenced ISO standards actually applies to a given programme is set by a nation's own procurement and the contract or tender in front of a supplier, not by this page. The standards explorer shows what else sits alongside AMedP-1.15, and we are glad to talk through what a specific tender or requirement is asking for.
Tell us how you need to work with AMedP-1.15 and what you need from it. We will come back to you about what ComplyTrain can do.
Thank you. Your list is on its way to your inbox, and we will come back to you on what working with these standards in ComplyTrain involves, usually within one business day.
It binds through STANAG 2178, the NATO agreement recording nations' commitment to use this publication; a nation can ratify with reservations. For an organisation, it typically arrives as a national or NATO contract or tender that names AMedP-1.15 or one of the connector families it covers.
No. AMedP-1.15 describes no certification, inspection or audit scheme of its own, and names no assessor. It is a technical connector-interface specification: conformity would be established by measuring a manufactured connector against the geometry the document sets, not by any process the document itself describes.
Yes. Annex A names ISO 80369-1 and ISO 80369-7 among the civil connector standards it sits alongside, covering small-bore connectors for liquids and gases in healthcare generally and, separately, connectors for intravascular or hypodermic applications. AMedP-1.15 does not state that meeting one standard satisfies the other.
STANAG 2178 is the NATO Standardization Agreement recording nations' commitment to use AMedP-1.15; AMedP-1.15 is the technical content itself, setting out the connector families and how they fit together. A nation ratifies the STANAG, with or without reservations, and that ratification is what gives AMedP-1.15 force for that nation.
No. AMedP-1.15 is a connector-interface specification. It does not set out patient care or treatment procedures, and this page does not describe any either; that content sits with national clinical protocols and appropriately qualified personnel, not with a connector standard.
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