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ISO 8836:2014
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Suction catheters for use in the respiratory tract |
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ISO 5360:2016
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Anaesthetic vaporizers Agent-specific filling systems |
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EN 15986:2011
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Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates |
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IEC 60601-1:2005+AMD1:2012 CSV
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Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
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IEC TR 60083:2015
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Plugs and socket-outlets for domestic and similar general use standardized in member countries of IEC |
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IEC 60601-1-6:2010+AMD1:2013 CSV
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Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
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BS 4272-3:1989
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Anaesthetic and analgesic machines Specification for continuous flow anaesthetic machines |
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ISO 13485:2016
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Medical devices Quality management systems Requirements for regulatory purposes |
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ISO 5356-1:2015
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Anaesthetic and respiratory equipment Conical connectors Part 1: Cones and sockets |
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ISO 9170-2:2008
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Terminal units for medical gas pipeline systems — Part 2: Terminal units for anaesthetic gas scavenging systems |
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ISO 10651-4:2002
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Lung ventilators — Part 4: Particular requirements for operator-powered resuscitators |
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IEC 60601-1-10:2007+AMD1:2013 CSV
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Medical electrical equipment - Part 1-10: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loopcontrollers |
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ISO 8835-7:2011
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Inhalational anaesthesia systems — Part 7: Anaesthetic systems for use in areas with limited logistical supplies of electricity and anaesthetic gases |
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ISO/TR 14969:2004
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Medical devices Quality management systems Guidance on the application of ISO 13485: 2003 |
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IEC 60079-20-1:2010
|
Explosive atmospheres - Part 20-1: Material characteristics for gas and vapour classification - Test methods and data |
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IEC 60601-1-8:2006+AMD1:2012 CSV
|
Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems |
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ISO 7396-2:2007
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Medical gas pipeline systems Part 2: Anaesthetic gas scavenging disposal systems |
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ISO 5145:2014
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Cylinder valve outlets for gases and gas mixtures Selection and dimensioning |
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ISO 5356-2:2012
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Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors |
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ISO 10079-1:2015
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Medical suction equipment Part 1: Electrically powered suction equipment |
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ISO 5367:2014
|
Anaesthetic and respiratory equipment — Breathing sets and connectors |
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IEC 60601-1-2:2014
|
Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
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ISO 5359:2014
|
Anaesthetic and respiratory equipment Low-pressure hose assemblies for use with medical gases |
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ISO 5362:2006
|
Anaesthetic reservoir bags |
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IEC 60079-11:2011
|
Explosive atmospheres - Part 11: Equipment protection by intrinsic safety "i" |
|
ISO 8185:2007
|
Respiratory tract humidifiers for medical use Particular requirements for respiratory humidification systems |
|
ISO/TR 16142:2006
|
Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices |
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IEC 62304:2006+AMD1:2015 CSV
|
Medical device software - Software life cycle processes |
|
ISO 3746:2010
|
Acoustics Determination of sound power levels and sound energy levels of noise sources using sound pressure Survey method using an enveloping measurement surface over a reflecting plane |
|
ASTM F 2761 : 2009 : R2013
|
Medical Devices and Medical Systems - Essential safety requirements for equipment comprising the patient-centric integrated clinical environment (ICE) - Part 1: General requirements and conceptual model |
|
IEC 60601-1-3:2008+AMD1:2013 CSV
|
Medical electrical equipment - Part 1-3: General requirements forbasic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment |
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ISO 2878:2017
|
Rubber, vulcanized or thermoplastic Antistatic and conductive products Determination of electrical resistance |
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ISO 80601-2-55:2011
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Medical electrical equipment Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors |
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ISO 10079-3:2014
|
Medical suction equipment Part 3: Suction equipment powered from a vacuum or positive pressure gas source |
|
ISO 407:2004
|
Small medical gas cylinders Pin-index yoke-type valve connections |
|
ISO 5358:1992
|
Anaesthetic machines for use with humans |
|
ISO 14155:2011
|
Clinical investigation of medical devices for human subjects Good clinical practice |
|
ISO 9170-1:2017
|
Terminal units for medical gas pipeline systems — Part 1: Terminal units for use with compressed medical gases and vacuum |
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ISO 14971:2007
|
Medical devices Application of risk management to medical devices |
|
ISO 4135:2001
|
Anaesthetic and respiratory equipment Vocabulary |
|
ISO 10524-1:2006
|
Pressure regulators for use with medical gases Part 1: Pressure regulators and pressure regulators with flow-metering devices |
|
ISO 594-2:1998
|
Conical fittings with 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 2: Lock fittings |
|
ISO 15223-1:2016
|
Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
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IEC 60601-1-9:2007+AMD1:2013 CSV
|
Medical electrical equipment - Part 1-9: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design |
|
IEC 60601-1-4:1996+AMD1:1999 CSV
|
Medical electrical equipment - Part 1-4: General requirements for safety - Collateral Standard: Programmable electrical medical systems |
|
ISO 7396-1:2016
|
Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum |