ASTM F 1101 : 1990 : R2003 : EDT 1
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Standard Specification for Ventilators Intended for Use During Anesthesia (Withdrawn 2012)
Hardcopy , PDF
31-03-2012
English
01-12-2003
CONTAINED IN VOL. 13.01, 2009 Applies to all ventilators specifically introduced for sale following acceptance of this specification and intended for use during the administration of anesthesia. Includes definitions, performance requirements, test methods and a rationale for all mandatory requirements.
Committee |
F 29
|
DocumentType |
Standard
|
Pages |
12
|
ProductNote |
Reconfirmed EDT 1
|
PublisherName |
American Society for Testing and Materials
|
Status |
Withdrawn
|
Supersedes |
1.1 This specification applies to all ventilators specifically introduced for sale following acceptance of this specification and intended for use during the administration of anesthesia. Definitions, performance requirements, test methods, and a rationale for all mandatory requirements are included.
1.2 The anesthesia ventilator cannot protect against malfunctions within the anesthesia machine, nor can it protect against inappropriate or inadvertent use of the oxygen flush valve, and therefore, no attempt has been made to address problems that may arise from malfunctions with these devices in this specification. (See also X3.1.)
1.3 Several definitions have been included in Section 2 and Appendix X1 that are not used in the text of this specification. This material has been included for the sake of completeness, and for any possible educational benefit that may be served. Appendix X1 also outlines various characteristics of ventilators intended for use during anesthesia and defines the main classes of breathing machines that may be used in medical practice and indicates how these may be subdivided according to their mode of action.
1.4 The following precautionary caveat pertains to the test methods portion, Section 6 of this specification. This standard may involve hazardous materials, operations, and equipment. This standard does not purport to address all of the safety concerns associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. For an additional safety precaution, see 7.1.7.
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IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ANSI Z79.11 : 1982 | SCAVENGING SYSTEMS FOR EXCESS ANESTHETIC GASES |
ANSI Z1979.10 : 1979 | OXYGEN ANALYZERS FOR MONITORING PATIENT BREATHING MIXTURES, REQUIREMENTS FOR, |
CGA V 5 : 2008(R2013) | DIAMETER INDEX SAFETY SYSTEM (NON-INTERCHANGEABLE LOW PRESSURE CONNECTIONS FOR MEDICAL GAS APPLICATIONS) |
ISO 4135:2001 | Anaesthetic and respiratory equipment Vocabulary |
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