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This specification covers reusable phase-change-type clinical thermometers for determination of human temperature. The following test method shall be performed for performance verification: accuracy test; operating environment test; storage environment test; toxicity test (extract); toxicity test (chemical ingestion); and cleaning tests.
This abstract is a brief summary of the referenced standard. It is informational only and not an official part of the standard; the full text of the standard itself must be referred to for its use and application. ASTM does not give any warranty express or implied or make any representation that the contents of this abstract are accurate, complete or up to date.
1.1 This specification covers reusable phase-change-type clinical thermometers.
1.2 The following safety hazards caveat pertains only to the test method portion, Section 6, of this specification. This standard does not purport to address all of the safety concerns, if any, 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.
2. Referenced Documents (purchase separately) The documents listed below are referenced within the subject standard but are not provided as part of the standard.
E344 Terminology Relating to Thermometry and Hydrometry
F895 Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
Code of Federal RegulationsCFR, Title 21, Section 191, II, 1971
ICS Number Code 17.200.20 (Temperature-measuring instruments)
UNSPSC Code 42182200(Medical thermometers and accessories)
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ASTM E1299-96(2010), Standard Specification for Reusable Phase-Change-Type Fever Thermometer for Intermittent Determination of Human Temperature, ASTM International, West Conshohocken, PA, 2010, www.astm.orgBack to Top