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ASTM F 984 : 1986 : R1992

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

Specification for Cutaneous Gas Monitoring Devices for Oxygen and Carbon Dioxide (Withdrawn 1999)

Withdrawn date

08-10-1999

Published date

31-12-2010

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CONTAINED IN VOL 13.01 1997 Outlines all devices used as non-invasive monitoring systems of the partial pressure of oxygen or carbon dioxide at the skin's surface.

Committee
F 29
DocumentType
Standard
PublisherName
American Society for Testing and Materials
Status
Withdrawn

1.1 This specification covers all devices intended for use as non-invasive monitoring systems of the partial pressure of oxygen or carbon dioxide at the skin's surface. This specification covers cutaneous monitors used with adults, children, and neonates, and may include the use of these devices in fetal monitoring prior to birth.

1.2 Current technology and clinical interpretative skills limit the primary application of these devices to indicate trends in the cutaneous partial pressure of oxygen and carbon dioxide, rather than to provide an absolute measurement.

1.3 Although the principal type of monitor in use at present involves the attachment of a sensor assembly with a heater to the skin's surface, this specification applies to all devices used to monitor partial pressure of gas at the skin's surface, regardless of the technique used to accomplish measurement.

1.4 This specification applies to devices manufactured following the adoption of this standard. This specification does not apply to hemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (that is, conjunctiva, mucosa).

1.5 The following precautionary caveat pertains only to the test method portion, Sections 10, 11, 12, and 13 of this specification: This standard may involve hazardous materials, operations, and equipment. This standard does not purport to address all of the safety problems associated with its use. It is the responsibility of whoever uses this standard to consult and establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

ASTM F 2002 : 2001 : REV A Standard Terminology Relating to Anesthesia and Respiratory Equipment
ASTM F 2002 : 2001 Standard Terminology Relating to Anesthesia and Respiratory Equipment
ASTM F 2002 : 2001 : REV B Standard Terminology Relating to Anesthesia and Respiratory Equipment
ASTM F 2002 : 2001C TERMINOLOGY RELATING TO ANESTHESIA AND RESPIRATORY EQUIPMENT

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