共找到 305 条与 医用材料 相关的标准,共 21 页
Test methods for nonwoven compresses for medical use - Part 1: Nonwovens used in the manufacture of compresses
This part of EN 1644 specifies physical and chemical tests for the evaluation of finished nonwoven compresses.
Test methods for nonwoven compresses for medical use - Part 2: Finished compresses
This part of EN 1644 specifies physical and chemical tests for the evaluation of finished nonwoven compresses.
Test methods for nonwoven compresses for medical use - Finished compresses
This document describes physical and chemical tests for the evaluation of finished compresses.
Test methods for nonwoven compresses for medical use - Part 2: Compresses; German version EN 1644-2:2000
This part of EN 1644 specifies physical and chemical tests forThe evaluation of finished nonwoven compresses.
Test methods for nonwoven compresses for medical use - Part 2: Finished compresses
This test method is used to evaluate the resistance of medical face masks to penetration by synthetic blood under high velocity liquid contact with the medical face mask surface of a fixed volume over a relatively short period of time (0 to 2.5 s). Medical face mask pass/fail determinations are based on visual detection of synthetic blood penetration This test method does not apply to all forms or conditions of blood-borne pathogen exposure. Users of the test method must review modes for face exposure and assess the appropriateness of this test method for their specific application. This test method primarily addresses the performance of materials or certain material constructions used in medical face masks. This test method does not address the performance of the medical face masks design, construction, or interfaces or other factors which may affect the overall protection offered by the medical face mask and its operation (such as filtration efficiency and pressure drop). Procedures for measuring these properties are contained in MIL-M-36954C. This test method does not address breathability of the medical face mask materials or any other properties affecting the ease of breathing through the medical face mask. This test method evaluates medical face masks as an item of protective clothing. This test method does not evaluate the performance of medical face masks for airborne exposure pathways or in the prevention of the penetration of aerosolized body fluids deposited on the medical face mask. The values stated in 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. 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.
Test Method for Resistance of Medical Face Masks to Penetration by Synthetic Blood (Horizontal Projection of Fixed Volume at a Known Velocity)
Standard Test Method for Determining Strength and Setting Time of Synthetic Water-Activated Polyurethane Fiberglass Orthopaedic Casting Tape
本标准规定了医疗器械制品中主要由医用高分子材料组成,且直接或间接作用于人体的制品术语。 本标准不包括人工器官术语。
Terminology relating to medical polymer products
本标准规定了医用高分子制品的包装、标志、运输和贮存。 本标准适用于医用高分子制品的包装、标志、运输和贮存。特殊制品由产品标准规定。
Package,lable,transport and storage for medical polymer products
Specifies requirements for menstrual tampons including length, pull strength and water repellency of the withdrawal cord, materials, absorptive capacity, microbial content, marking and packaging. Includes a classification system based on tampon absorbency with descriptive terms to be used in labelling tampons according to their absorbency range. Information to be given in an accompanying leaflet is described.
Tampons - Menstrual
This part of the standard specifies physical and chemical test methods for the evaluation of nonwovens used as materials for compresses for medical use.
Test methods for nonwoven compresses for medical use - Part 1: Nonwovens used in the manufacture of compresses
Настоящий стандарт распространяется на медицинские эластичные фиксирующие и компрессионные изделия [бинты, бандажи, чулочно-носочные из
Manufactured articles medical elasticity for the fixation and compression. General technical requirements. Test methods
This Part of EN 1644 specifies physical and chemical test methods for the evaluation of nonwovens used as materials for compresses for medical use.
Test methods for nonwoven compresses for medical use - Nonwovens used in the manufacture of compresses
Test methods for nonwoven compresses for medical use. Part 1 : nonwovens used in the manufacture of compresses.
This document describes physical and chemical tests for the evaluation of nonwovens used as materials for compresses for medical use.
Test methods for nonwoven compresses for medical use - Part 1: Nonwovens used in the manufacture of compresses; German version EN 1644-1:1997
This Part of EN 1644 specifies physical and chemical test methods for the evaluation of nonwovens used as materials for compresses for medical use
Test methods for nonwoven compresses for medical use - Part 1: Nonwovens used in the manufacture of compresses
This British Standard specifies requirements for flat, non-adhesive,extensible bandages manufactured from wiven or knitted fabtics them according to their function and performance.
Specification for the elastic properties of flat, non- adhesive, extensible fabric bandages
本标准规定了药用铝瓶的产品分类、技术要求、试验方法、检验规则和标志、包装、运输、贮存的要求。 本标准适用于装抗生索原料药粉剂的药用铝瓶。
Aluminum bottle for medicines
5.1 Diametral compression strength is an important measure of the mechanical properties of casting materials. This test method simulates the loading pattern seen in lower extremity casting applications during ambulation. This test method cannot be used to determine cast life or measure bending or other modes of cast failure. 5.2 This test method measures but does not prescribe values. 1.1 This test method covers the functional diametral compression strength of cylindrical test specimens formed from synthetic fiberglass polyurethane casting materials. The test specimens employed in this test method are similar in geometry and construction to casts used in orthopaedic applications. This test method is not intended to determine the strength of the base materials used for fabrication of the test specimen. 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 and health practices and determine the applicability of regulatory limitations prior to use. Specific warning statements are given in 6.7.
Standard Test Method for Determining Strength and Setting Time of Synthetic Water-Activated Polyurethane Fiberglass Orthopaedic Casting Tape
Diametral compression strength is an important measure of the mechanical properties of casting materials. This test method simulates the loading pattern seen in lower extremity casting applications during ambulation. This test method cannot be used to determine cast life or measure bending or other modes of cast failure. This test method measures but does not prescribe values.1.1 This test method covers the functional diametral compression strength of cylindrical test specimens formed from synthetic fiberglass polyurethane casting materials. The test specimens employed in this test method are similar in geometry and construction to casts used in orthopaedic applications. This test method is not intended to determine the strength of the base materials used for fabrication of the test specimen. 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 and health practices and determine the applicability of regulatory limitations prior to use. Specific warning statements are given in 6.7.
Standard Test Method for Determining Strength and Setting Time of Synthetic Water-Activated Polyurethane Fiberglass Orthopaedic Casting Tape
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