3.1 The objective of surface treatments as documented in this practice is to improve the corrosion resistance of metallic surgical implants including, but not limited to, those manufactured from iron, cobalt, nickel, titanium, and tantalum base materials.3.2 Iron particles, ceramic media, and other foreign particles may become smeared over or embedded into the surface of implants during processing operations such as forming, machining, tumbling, media blasting, marking, and so forth. These particles should be removed to minimize localized corrosion and superficial blemishes.3.3 The various chemical and electrochemical surface treatments specified by this practice are used to remove objectionable surface contaminants and to restore maximum corrosion resistance to, or promote the creation of, an inert or passive surface, such as a metal oxide film, as is applicable to the specific material. Some of these treatments are referred to as passivation treatments. The preferred surface treatment for a given application varies depending on the implant material and the nature of the surface contaminants.3.4 Depending on the implant, its material, and the type of marking method and procedure, the marking may be applied before or after a chemical or electrochemical surface treatment. When marking is performed after the surface treatment, the localized implant surface shall be evaluated to determine if there is a need for additional surface treatment.NOTE 1: The need for additional surface treatment is likely for stainless steel with all marking methods, and for nonferrous alloys when the marking method involves direct or second-hand contact with iron-based or other material that would be considered an objectionable surface contaminant.3.5 The selection of procedures to be applied to the implants, and additional requirements which are not covered by this practice, may be included in the implant production specification.1.1 This practice provides descriptions of surface characteristics, surface preparation, and marking for metallic surgical implants, with the purpose of improving the corrosion resistance of the implant surfaces and markings.1.2 Marking nomenclature and neutralization of endotoxin are not specified in this practice (see X1.4).1.3 Surface requirements and marking methods included in the implant specification shall take precedence over requirements listed in this practice, where appropriate.1.4 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in nonconformance with the standard.1.5 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.1.6 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.

定价： 590元 / 折扣价： 502 元 加购物车

4.1 The following practices are to be used in obtaining samples that are representative of the lot being sampled. The methodology used will be dependent upon the size and type of material sampled and testing requirements.4.2 The following practices are intended for use in obtaining samples from material that is ready for sale and are not intended as sampling procedures for quality control purposes. These practices are to be used in obtaining a laboratory sample that will yield results serving as a basis for acceptance or rejection of the lot of material sampled. This does not preclude the use of these practices for quality control purposes.4.3 The following practices can be used to eliminate bias in sampling. The person or persons responsible for using these practices must be trained and they will be conscientious and timely in their use.4.4 An agreement between the producer and the consumer on location of sampling, either at the producer's plant or at the destination, is encouraged. Product quality can be affected through careless handling, improper protection, and delayed shipment. It is preferable to sample at the point of loading. The consumer has the right to witness the sampling practices being used.4.5 This practice may be used to provide a representative sample of lime or limestone products. Due to the variability of limestone and lime and the wide variety of sampling equipment, caution must be exercised in all stages of sampling, from system specification and equipment procurement to equipment acceptance testing and actually taking the final sample.1.1 This practice covers procedures for the collection and reduction of samples of lime and limestone products to be used for physical and chemical tests.1.2 This practice further covers inspection, rejection, retesting, packing, and marking of lime and limestone products as it may be used in the chemical, agricultural, and process industries.1.3 The values stated in either SI units or inch-pound units are to be regarded separately as standard. Within the text, the inch-pound units are shown in brackets. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard.1.4 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.1.5 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.

定价： 590元 / 折扣价： 502 元 加购物车

5.1 The drying rate of organic coatings varies with changes in temperature, air flow, and relative humidity. In particular, the drying rate of waterborne paints depends on the evaporation of water and thus is much more dependent on relative humidity than are solvent based paints or paints that are 100 % solids. Measurement of the rate of drying of waterborne paints under ambient conditions in laboratories cannot be adequately replicated without some control of the drying conditions. A test chamber will be described that provides a means of controlling relative humidity above ambient humidity and minimizing the effects of air flow variability at ambient room temperatures. If desired, the test chamber without water in it and with vents wide open can be placed in a temperature and humidity controlled room to test dry speed at various temperatures as well as humidity while using the chamber to minimize the effect of air flow.5.2 This practice is particularly useful for testing the drying rate of waterborne pavement marking (traffic) paints where fast dry at elevated ambient humidity is an important feature. For waterborne traffic paints, the test chamber can be used to evaluate dry to no-pick-up (Test Method D711) and water wash-off resistance (Practices D7377 and D7538) at elevated ambient humidity.1.1 Specification D3924 defines a standard environment of 23 ± 2°C and 50 ± 5 % relative humidity and free from drafts for normal conditioning and testing of paint, varnish, lacquer, and related materials. This practice describes a test chamber that allows for control of relative humidity above the ambient relative humidity and minimization of air flow for conditioning of test panels at elevated relative humidity and room temperatures.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.

定价： 590元 / 折扣价： 502 元 加购物车

4.1 Interactions of items with the MR environment have resulted in serious injuries and death of patients and other individuals. This practice lists hazards that may be present in the MR environment. It specifies marking of items anticipated to enter the MR environment and recommends information that should be included in the associated labeling.4.2 This practice provides a uniform system of visual icons and terms for marking items for use in the MR environment.1.1 This practice applies to medical devices and other items that are anticipated to enter the magnetic resonance (MR) environment.NOTE 1: “Medical devices and other items” will be referred to as “items” for the remainder of this practice.1.2 The practice specifies the marking of items anticipated to enter the MR environment by means of terms and icons, and recommends information that should be included in the labeling.1.3 MR image artifacts are not in the scope of the mandatory portions of this practice because they do not present a direct safety issue resulting from specific characteristics of the MR examination (see X1.12).1.4 The values stated in SI units are to be regarded as standard.1.5 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.1.6 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.

定价： 646元 / 折扣价： 550 元 加购物车