1.1 This guide establishes the minimum training standard for emergency medical technicians (basic) as it relates to their roles and responsibilities. 1.2 This guide is one of a series which together describe the minimum training standard for the emergency medical technician (basic). 1.3 This standard does not purport to address all of the safety problems, 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.

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1.1 This guide establishes the minimum national standard for training in the management of shock in patients of all ages by the emergency medical technician (basic). 1.2 This guide is one of a series which together describe the minimum training standard for the emergency medical technician (basic). 1.3 This standard does not purport to address all of the safety problems, 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.

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1.1 This guide establishes the minimum national standard for training the emergency medical technician (basic) to perform patient management techniques for patients of all ages. 1.2 This guide is one of a series which together describe the minimum training standard for the emergency medical technician (basic). 1.3 This standard does not purport to address all of the safety problems, 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.

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This specification covers basic carbonate white lead used as a pigment and in putty. The pigments may be in dry form or a paste in oil. Dry pigment shall conform to the required contents of lead carbonate, moisture and other volatile matter, impurities, and coarse particles. Paste in oil and semipaste containing volatile thinner shall also conform to the requirements of pigment, linseed oil, moisture and other volatile matter, and coarse particles and skins of dry pigment. Tests for the following shall be done: coarse particles; moisture in pigment; lead carbonate and total other impurities; and pigment, linseed oil, and moisture and other volatile matter in paste in oil.1.1 This specification covers the material commercially known as basic carbonate white lead, used as a pigment and in putty. The pigment may be purchased in the dry form or as a paste in oil.1.2 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.1.3 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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1.1 This guide establishes the minimum training standard for the management of Obstetrical Emergencies by the emergency medical technician (basic). 1.2 This guide is one of a series which together describe the minimum training standard for the emergency medical technician (basic). 1.3 This standard does not purport to address all of the safety problems, 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.

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This specification covers rotary wing aircraft involved in patient prehospital emergency medical care and transportation. It outlines the minimum requirements, including personnel, and patient care equipment and supplies, that must be met before the aircraft can be classified as a rotary wing air ambulance unit. This specification describes a suitable rotary wing aircraft, which together with the specified personnel, equipment, and supplies, will provide patient care, at least to national standards for basic life support, throughout the medical mission. It applies to all the medical activities that involve rotary wing air ambulance operation at the basic life support level, including on-scene work and interhospital transfer. Application of this specification will ensure that the air ambulance will be able to provide a well-established level of patient care. The rotary wing basic life support air ambulance shall consist of three components: the rotary wing medical transport vehicle, transport personnel, and patient care equipment and supplies in accordance with this specification. The minimum personnel requirement for the rotary wing basic life support air ambulance shall be the FAA flight crew requirement for the aircraft and for each patient, one qualified air-medical crewmember. All pieces of medical equipment and supplies used in rotary wing operations shall be maintained in accordance with the specified requirements.1.1 This specification pertains to fixed (airplanes) and rotary-wing (helicopters) aircraft used for prehospital emergency medical care and transportation of patients by air, collectively air ambulances. It outlines the minimum requirements, including personnel, patient care equipment, and supplies that shall be met before the aircraft can be classified as an air ambulance.1.2 Recommendations for basic life support (BLS) air ambulances are contained in the first part of this specification that defines the minimum requirements for aircraft configuration and capability, the minimum number of seats for personnel, and the minimum medical equipment and supplies.1.3 Recommendations for advanced life support (ALS) air ambulances include the first part of this specification that defines the minimum requirements for aircraft configuration and capability, the minimum number of seats for personnel, and the minimum medical equipment and supplies. Additional requirements for ALS are found in Annex A1.1.4 Recommendations for specialized medical support (SMS) air ambulances include those for BLS and may include some or all of the ALS requirements that define the minimum requirements for aircraft configuration and capability, the minimum number of seats for personnel, and the minimum medical equipment and supplies. Additional requirements for SMS air ambulances are found in Annex A2.1.5 In this specification, minimum requirements for air ambulances providers are identified, however, ambulance services, under the direction of their medical director, are encouraged to use them as a core list and adjust their configuration or manifest or both according to their mission profile and patient population.1.6 Units—The values stated in inch-pound units are to be regarded as the standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.1.7 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.

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This specification pertains to fixed wing aircraft (airplanes) used for patient prehospital emergency medical care and transportation. It describes the minimum aircraft configuration and capability, the minimum number of seats for personnel, and the provisions for the minimum medical equipment and supplies for fixed wing basic life support air ambulances. This will also assist in the definition of appropriate care, increase public awareness of the high standard available, and provide a nationally accepted guideline. The fixed wing basic life support air ambulance shall consist of three components: the fixed wing medical transport vehicle (airplane), transport personnel, and patient care equipment and supplies The three components must be licensed/certified by the appropriate governmental authority.1.1 This specification pertains to fixed wing aircraft (airplanes) used for patient prehospital emergency medical care and transportation. It outlines the minimum requirements, including personnel, and patient care equipment and supplies, that must be met before the aircraft can be classified as a fixed wing air ambulance unit.1.2 The first part of this specification (Sections through ) describes the minimum aircraft configuration and capability, the minimum number of seats for personnel, and the provisions for the minimum medical equipment and supplies for fixed wing basic life support air ambulances.1.3 The provisions of this specification plus the provisions of the Advanced Life Support (ALS) Annex comprise the specification for fixed wing advanced life support air ambulances. See Sections 1 and 1.1 of the Advanced Life Support (ALS) Annex for the scope for fixed wing advanced life support air ambulances.1.4 The provisions of this Sspecification plus the provisions of the Advanced Life Support Annex, plus the provisions in this Specialized Medical Support (SMS) Annex comprise the specification for fixed wing specialized medical support air ambulances. See Sections 1 through 1.3 of the Specialized Medical Support (SMS) Annex for the scope for fixed wing specialized medical support air ambulances.

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4.1 The acidity of a chrome tanning liquor, as determined by this test method, is rarely employed as such. This result is normally combined with the results of a chromium analysis (see Test Method D3898) to determine a property of the liquor called basicity. This property, equal to the percentage by which anions in a normal chromic salt have been replaced by hydroxyl in the solution being analyzed, is closely related to the tanning behavior of the solution.1.1 This test method covers the determination of the titratable acidity of chromium tanning liquors. By titratable acidity is meant not only free acidity, which is rarely present, but also anions combined with weakly basic cations such as Chromium (III), which can be titrated with base at the phenolphthalein end point.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 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, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 The procedure described is for the quality control for manufacturing liquors and specifications for the purchase of such liquors.4.2 The chromium content of the liquors determines the amount to be used to obtain the desired degree of tannage, and hence may be a matter for specification in the purchase of leather.1.1 This test method covers the determination of chromic oxide in chrome tanning liquors, either simple, with added aluminum or zirconium, or with the usual masking complexing agents.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 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, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This specification establishes the requirements and test methods for the material, dimensions, and workmanship, and the physical and electrical properties of molded sheet manufactured from polytetrafluoroethylene (PTFE) resin molding materials and molded basic shapes made from resin molding and extrusion materials. The sheet or molded basic shape shall be made from unpigmented PTFE and shall be free from foreign matters. Each of the samples shall undergo visual and dimensional inspection to verify their compliance with the standard requirements. The specimens shall conform to the following physical and electrical property requirements: tensile strength; elongation; dielectric strength; specific gravity; porosity; and melting point. Examination for internal defects shall also be conducted to ensure that the specimens are free from microscopic cracks, voids, inclusions, and other surface defects that might affect the serviceability of the materials.1.1 This specification establishes requirements and methods of test for the material, dimensions, and workmanship, and the physical and electrical properties of molded sheet in minimum thicknesses of 0.794 mm (1/32 in.) manufactured from PTFE resin molding materials defined in Specification D4894.1.2 This specification also establishes requirements for molded basic shapes made from molding materials. This specification is for products 300 mm (12 in.) or less in a dimension parallel to and 12.7 mm (0.5 in.) or greater in the dimension perpendicular to the direction of the applied molding pressure.1.3 The values stated in SI units are to be regarded as the standard.1.4 The following precautionary caveat pertains only to the test method portion, Section 7, 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, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Special attention is called to 13.2, 13.3, 13.6, 13.8, and A1.NOTE 1: There is no known ISO equivalent to this standard.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 This practice defines a procedure that ensures reasonably consistent preparation of specimens for product testing and evaluation.4.2 This practice can be used in the laboratories of producers, users, and general interest parties for research and development or quality control work. It is particularly useful for interlaboratory comparisons on products, for repetitive evaluations or comparisons of products or product quality, and in specifying a uniform preparation practice for specimens for acceptance testing.4.3 If pitch-impregnated samples are prepared by wet cutting or drilling, care should be taken in drying them. If the samples are heated to facilitate drying, the temperature to which they are heated should not be so high that it causes drainage of pitch from the samples.4.4 Porosities of metal-containing brick must be measured using kerosene or mineral spirits, because using water will result in an artificially low result.1.1 This practice covers a procedure for preparing test specimens from magnesia-carbon and impregnated burned basic brick. This practice generally concerns preparation of test specimens from brick greater than 13 in. (33 cm) in length. These brick are mainly manufactured for use in electric arc furnaces and basic oxygen furnaces.1.2 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.1.3 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, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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1.1 This specification pertains to rotary wing transport units involved in patient transportation and care at the basic life support level. It outlines the minimum requirements, including personnel, and the patient care equipment and supplies, that must be met before the unit can be classified as an basic life support transport unit. 1.2 This specification describes; the minimum vehicle configuration and capability, the minimum number of seats for personnel, and the provisions for the minimum medical equipment and supplies. 1.3 Other specifications of Committee F-30 will apply.

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