BS ISO 10651-5:2006
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Lung ventilators for medical use. Particular requirements for basic safety and essential performance Gas-powered emergency resuscitators
08-13-2021
05-30-2008
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
4.1 General
4.2 Other test methods
4.3 Acceptance criteria
5 Constructional requirements
5.1 General
5.2 Connectors
6 Operational requirements
6.1 General
6.2 Resistance to environmental influences
6.3 Resistance to typical use
6.4 Size and mass
6.5 Gas supply
7 Performance
7.1 Ventilatory requirements
7.2 Ventilation performance
8 Identification, marking and documents
8.1 General
8.2 Marking
8.3 Information provided by the manufacturer for
operation and maintenance
Annex A (informative) - Rationale
Annex B (normative) - Test methods
Annex C (informative) - Relationship between this part of
ISO 10651 and cardiopulmonary
resuscitation guidelines
Annex D (informative) - Clauses of this part of ISO 10651
addressing the essential principles
Annex E (informative) - Terminology - Index of defined
terms
Bibliography
Describes the basic safety and essential performance requirements for gas-powered emergency resuscitators intended for use with humans by first responders.
| Committee |
CH/121/9
|
| DevelopmentNote |
Supersedes 04/30088362 DC. (05/2008)
|
| DocumentType |
Standard
|
| PublisherName |
British Standards Institution
|
| Status |
Withdrawn
|
| Supersedes |
| Standards | Relationship |
| ISO 10651-5:2006 | Identical |
| ISO/IEC TR 10000-1:1998 | Information technology — Framework and taxonomy of International Standardized Profiles — Part 1: General principles and documentation framework |
| ISO 10241:1992 | International terminology standards Preparation and layout |
| ISO 690:2010 | Information and documentation Guidelines for bibliographic references and citations to information resources |
| ISO 11135:2014 | Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| ISO 5356-1:2015 | Anaesthetic and respiratory equipment Conical connectors Part 1: Cones and sockets |
| ISO 14937:2009 | Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
| ISO 5356-2:2012 | Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors |
| ISO 32:1977 | Gas cylinders for medical use — Marking for identification of content |
| ISO 5367:2014 | Anaesthetic and respiratory equipment — Breathing sets and connectors |
| ISO 690-2:1997 | Information and documentation Bibliographic references Part 2: Electronic documents or parts thereof |
| ISO 10297:2014 | Gas cylinders — Cylinder valves — Specification and type testing |
| ISO 5359:2014 | Anaesthetic and respiratory equipment — Low-pressure hose assemblies for use with medical gases |
| ISO 10524-3:2005 | Pressure regulators for use with medical gases Part 3: Pressure regulators integrated with cylinder valves |
| ISO 23328-2:2002 | Breathing system filters for anaesthetic and respiratory use — Part 2: Non-filtration aspects |
| IEC 60027-3:2002 | Letter symbols to be used in electrical technology - Part 3: Logarithmic and related quantities, and their units |
| IEC 60529:1989+AMD1:1999+AMD2:2013 CSV | Degrees of protection provided by enclosures (IP Code) |
| ISO 11607:2003 | Packaging for terminally sterilized medical devices |
| ISO 23328-1:2003 | Breathing system filters for anaesthetic and respiratory use — Part 1: Salt test method to assess filtration performance |
| IEC 60027-2:2005 | Letter symbols to be used in electrical technology - Part 2: Telecommunications and electronics |
| ISO 9170-1:2017 | Terminal units for medical gas pipeline systems — Part 1: Terminal units for use with compressed medical gases and vacuum |
| ISO 11134:1994 | Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization |
| IEC 60027-4:2006 | Letter symbols to be used in electrical technology - Part 4: Rotating electric machines |
| 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 11137:1995 | Sterilization of health care products Requirements for validation and routine control Radiation sterilization |
| EN 980:2008 | Symbols for use in the labelling of medical devices |
| ISO 17664:2017 | Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
| ISO 15223:2000 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied |
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