11.040.50 射线照相设备 标准查询与下载



共找到 1767 条与 射线照相设备 相关的标准,共 118

本标准规定了采用声弹性体模检测准静态超声应变弹性成像性能的术语、定义、试验装置以及方法。 本标准适用于采用超声回波成像原理的人体组织准静态应变弹性成像。

Ultrasound.Test methods of performance for quasi-static strain sonoelasticity

ICS
11.040.50
CCS
C41
发布
2016-01-26
实施
2017-01-01

本标准规定了医用超声耦合剂的定义、分类、要求、试验方法、检验规则及其包装、标志、运输和贮存。 本标准适用于医用超声耦合剂产品(以下简称产品),包括企业作为商品制造、销售的,也包括医疗机构自制自用的。该产品在超声诊断和治疗操作中用作探头、治疗头与人体组织之间的透声媒质。

Medical ultrasonic couplants

ICS
11.040.50
CCS
C41
发布
2016-01-26
实施
2018-01-01

本标准规定了口腔X射线数字化体层摄影设备在制造商规定的医疗使用条件下,进行颌骨骨密度测定的评价方法。本标准的预期使用者是制造商、医院和测试实验室。 本标准适用于制造商声称具有骨密度测量功能的口腔X射线数字化体层摄影设备。

Oral cavity X-ray equipment for digital tomography.Evaluation method for determination of bone mineral density

ICS
11.040.50
CCS
C43
发布
2016-01-26
实施
2017-01-01

本标准规定了医用超声设备(系统)(以下简称设备或系统)环境试验的特殊试验要求和试验方法。本标准的目的是评价设备或系统在规定的各种不同试验环境条件下的适应性。本标准适用于所有医用超声设备(系统)。

Environmental requirement and test methods for medical ultrasonic equipment

ICS
11.040.50
CCS
C41
发布
2016-01-26
实施
2017-01-01

Medical electrical equipment. Flat-panel digital X-Ray detectors. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. Medical X-Ray Film Processor. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Perangkat elektromedik - Bagian 2-27: Persyaratan khusus untuk keselamatan dasar dan kinerja esensial peralatan monitor elektrokardiografik

ICS
11.040.50
CCS
发布
2016
实施

Medical electrical equipment. Dental intra-oral X-ray equipment. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. Pediatric X-ray equipment for digital radiography. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. Radiology workstation. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. Universal Radiographic Digital Systems. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. Mobile digital X-ray Unit. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. H-Ray Bone Densitometer (Absorptiometer). Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. Computed radiography systems. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. X-Ray systems for digital radiography and tomosynthesis. Technical requirements for governmental purchases

ICS
11.040.50
CCS
发布
2016
实施
2017-09-01

Medical electrical equipment. Particular requirements for the basic safety and essential performance of endoscopic equipment

ICS
11.040.50
CCS
C39
发布
2015-11-30
实施
2015-11-30

Medical electrical equipment - Characteristics of digital x-ray imaging devices - Part 1-1: Determination of the detective quantum efficiency - Detectors used in radiographic imaging (IEC 62220-1-1:2015)

ICS
11.040.50
CCS
发布
2015-11-16
实施

IEC 61675-2:2015 specifies terminology and test methods for describing the characteristics of gamma cameras equipped with parallel hole collimators for planar imaging. This second edition of IEC 61675-2 cancels and replaces the first edition published in 1998 and its Amendment 1 published in 2004, as well as IEC 60789:2005, IEC 60789:2005/COR1:2009, and IEC 61675-3:1998. It has been reformatted, updated, and partly aligned with NEMA NU 1-2007.

Radionuclide imaging devices - Characteristics and test conditions - Part 2: Gamma cameras for planar, wholebody, and SPECT imaging

ICS
11.040.50
CCS
发布
2015-11-06
实施
2015-12-10 (7)

Radiotherapy equipment - Coordinates, movements and scales (IEC 61217:2011); German version EN 61217:2012

ICS
11.040.50
CCS
C43
发布
2015-11
实施

IEC 62467-1:2009 specifies the performance and some related constructional requirements of well-type ionization chambers and associated measurement apparatus, intended for the determination of a quantity, such as air kerma strength or reference air kerma rate in photon radiation fields or absorbed dose to water at a depth, in photon and beta radiation fields used in brachytherapy, after appropriate calibration for a given type of source. IEC 62467-1:2009 covers the techniques for the quantification of the quantity appropriate for the brachytherapy source under consideration. This quantity may be air kerma strength or reference air kerma rate at 1 m, or absorbed dose to water at a depth (e.g. 2 mm or 5 mm). Measurement of these quantities may be accomplished by a variety of well-type ionization chambers or systems currently available for this purpose. This standard applies to products intended for low dose rate, high dose rate, intravascular, both photon and beta, brachytherapy measurements. It does not apply to instruments for nuclear medicine applications. The application of the standard is limited to instruments that incorporate well-type ionization chambers as detectors. The intended use is the measurement of the output of radioactive, encapsulated sources for intracavitary (insertion into body cavities) or interstitial (insertion into body tissue) applications. The object of IEC 62467-1:2009 is a) to establish requirements for a satisfactory level of performance for well-type chamber systems, and b) to standardize the methods for the determination of compliance with this level of performance. IEC 62467-1:2009 is not concerned with the safety aspects of well-type chamber systems. The well-type chamber systems covered by this standard are not intended for use in patient environment. The electrical safety of well-type chamber systems is covered in IEC 61010-1. The operation of the electrometer measuring system is covered in IEC 60731.

Medical electrical equipment - Dosimetric instruments as used in brachytherapy - Part 1: Instruments based on well-type ionization chambers

ICS
11.040.50
CCS
发布
2015-10-23
实施
2015-12-15 (7)



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