C37 医疗设备通用要求 标准查询与下载



共找到 713 条与 医疗设备通用要求 相关的标准,共 48

Applies to electromagnetic compatibility of medical electrical equipment and medical electrical systems, hereinafter referred to as equipment and systems, respectively. Specifies requirements and tests for electromagnetic compatibility of equipment and s

Medical electrical equipment Part 1-2: General requirements for safety - Collateral standard: Electromagnetic compatibility - Requirements and tests

ICS
11.040.01;33.100.01
CCS
C37
发布
2005-05-12
实施

This specification is approved for use by all Departments and Agencies of the Department of Defense.

VECTOR PRODUCT FORMAT (VPF) PRODUCTS, GENERAL SPECIFICATION FOR

ICS
CCS
C37
发布
2005
实施

1.1 This practice establishes essential and recommended elements in the design, conduct, and reporting of research on psychophysiological detection of deception (polygraph) (PDD). Analog and field research are addressed separately. 1.2 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.

Standard Practice for Conduct of Research in Psychophysiological Detection of Deception (Polygraph)

ICS
11.040.55
CCS
C37
发布
2005
实施

1.1 This practice establishes essential and recommended elements in the design, conduct, and reporting of research on psychophysiological detection of deception (polygraph) (PDD). Analog and field research are addressed separately.

Standard Practice for Conduct of Research in Psychophysiological Detection of Deception (Polygraph)

ICS
11.040.55
CCS
C37
发布
2005
实施

Le Conseil canadien des normes est l’organisme de coordination du Système de Normes nationales, une fédération d’organismes indépendants et autonomes qui travaillent au développement et à l’amélioration de la normalisation volontaire dans l’intérêt na

Medical electrical equipment - Part 1-6: General requirements for safety - Collateral Standard: Usability First Edition; IEC 60601-1-6: 2004

ICS
CCS
C37
发布
2005
实施

Specifies strategies for hazard identification and tests on medical devices for the following biological aspects: genotoxicity, carcinogenicity, and reproductive and developmental toxicity. This part of SANS 10993 is applicable for evaluation of a medical device whose potential for genotoxicity, carcinogenicity or reproductive toxicity has been identified.

Biological evaluation of medical devices Part 3: Test for genotoxicity, carcinogenicity and reproductive toxicity

ICS
11.100
CCS
C37
发布
2004-12-15
实施

Specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical d

Medical devices - Quality management systems - Requirements for regulatory purposes

ICS
11.040.01
CCS
C37
发布
2004-11-19
实施

In vitro diagnostic medical devices - Single-use receptables for the collection of specimens, other than blood, from humans.

ICS
11.100.10
CCS
C37
发布
2004-10-01
实施
2004-10-20

Laboratory medicine - Requirements for reference measurement laboratories.

ICS
11.100.01
CCS
C37
发布
2004-09-01
实施
2004-09-20

L’Association canadienne de normalisation (CSA), sous les auspices de laquelle cette Norme nationale a été préparée, a re?u ses lettres patentes en 1919 et son accréditation au sein du Système de Normes nationales par le Conseil canadien des normes en

Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment First Edition

ICS
CCS
C37
发布
2004-07-01
实施

Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-010: Particular requirements for laboratory equipment for the heating of materials Second Edition; IEC 61010-1-010:2003

Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-010: Particular requirements for laboratory equipment for the heating of materials Second Edition

ICS
CCS
C37
发布
2004-07-01
实施

L’Association canadienne de normalisation (CSA), sous les auspices de laquelle cette Norme nationale a été préparée, a re?u ses lettres patentes en 1919 et son accréditation au sein du Système de Normes nationales par le Conseil canadien des normes en

Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-032:Particular requirements for hand-held and hand-manipulated current sensors for electrical test and measurement Second Edition

ICS
CCS
C37
发布
2004-07-01
实施

Provides general requirements for evaluating the interactions of medical devices with blood. It describes a classification of medical and dental devices that are intended for use in contact with blood, the fundamental principles governing the evaluation of the interaction of devices with blood, the rationale for structured selection of tests according to specific categories and the principles and scientific basis of these tests. It describes biological evaluation in general terms and may not necessarily provide sufficient guidance for test methods for a specific device.

Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood

ICS
11.100
CCS
C37
发布
2004-04-08
实施

Although the intended primary application of this standard is stated in its scope, it is important to note that it remains the responsibility of the users of the standard to judge its suitability for their particular purpose.

Medical electrical equipment ?Part 2-51: Particular requirements for safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs First Edition

ICS
CCS
C37
发布
2004-04-01
实施

The Canadian Standards Association (CSA), under whose auspices this National Standard has been produced, was chartered in 1919 and accredited by the Standards Council of Canada to the National Standards system in 1973. It is a not-for-profit, nonstat

Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment First Edition

ICS
CCS
C37
发布
2004-04-01
实施

The purpose of this notice is to inform users of the change in name of the preparing activity from the Defense and Mapping Agency (DMA) to the National Geospatial-Intelligence Agency(NGA).

REGISTERED DATA VALUES FOR RASTER PRODUCT FORMAT

ICS
CCS
C37
发布
2004-03-31
实施

The purpose of this notice is to inform users of the change in name of the preparing activity from the Defense and Mapping Agency (DMA) to the National Geospatial-Intelligence Agency (NGA).

VECTOR PRODUCT FORMAT [Superseded: DOD MIL-STD-600006 ADMIN NOTICE 2, DOD MIL-STD-600006 NOTICE 1, DOD MIL-STD-600006]

ICS
CCS
C37
发布
2004-03-31
实施

The purpose of this notice is to inform users of the change in name of the preparing activity from the National Imagery and Mapping Agency (NIMA) to the National Geospatial-Intelligence Agency (NGA), effective 24 October 2003.

BAR CODING FOR GEOSPATIAL PRODUCTS

ICS
CCS
C37
发布
2004-03-31
实施

Users should refer corrections, additions, and comments to the NGA Operational Help Desk: 1-800-455-0899; commercial 314-263-4864; DSN 693-4864; or write to: Director, National Geospatial-Intelligence Agency, ATTN: ES, Mail Stop L-88, 4600 Sangamore Road

WORLD MAGNETIC MODEL (WMM)

ICS
CCS
C37
发布
2004-03-31
实施

MIL-N-89404 remains inactive for new design (see NOTICE 1).

NON-SIOP OPTION (NSO) SUPPORT

ICS
CCS
C37
发布
2004-03-31
实施



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