ISO 5366 First edition 2016-10-01

Standard Organization:

ISO 5366 First edition 2016-10-01
Anaesthetic and respiratory equipment - Tracheostomy tubes and connectors

Recognition Date2019-01-14
Recognition List051
Recognition Number1-117
Extent Complete standard
Standards Orgs ISO International Organization for Standardization https://www.iso.org/
STG Anesthesiology

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:

ISO 5366:2016 specifies requirements for adult and paediatric tracheostomy tubes and connectors. Such tubes are primarily designed for patients who require anaesthesia, artificial ventilation or other respiratory support.

ISO 5366:2016 is also applicable to specialized tracheostomy tubes that share common attributes, for example, those without a connector at the machine end intended for spontaneously breathing patients and those with reinforced walls or tubes made of metal or tubes with shoulders, tapering tubes, tubes with provision for suctioning or monitoring or delivery of drugs or other gases.

Flammability of tracheostomy tubes is a well recognized hazard (for example, when electrosurgical units or lasers are used with flammable anaesthetic agents in oxidant-enriched atmospheres) that is addressed by appropriate clinical management and is outside the scope of this International Standard.

NOTE ISO/TR 11991 gives guidance on avoidance of airway fires.

Code of Federal Regulations:

Regulation Number Device Name Device Class Product Code
§868.5800 Tube Tracheostomy And Tube Cuff Class 2 JOH
§868.5800 Tube, Tracheostomy (W/Wo Connector) Class 2 BTO
§868.5730 Tube, Tracheal (W/Wo Connector) Class 2 BTR

FDA Guidance:

Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling - Guidance for Industry and Food and Drug Administration Staff, Issued March 2015.


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