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 页
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VECTOR PRODUCT FORMAT [Superseded By: DOD MIL-STD-2407 ADMIN NOTICE 2, DOD MIL-STD-2407 CHG NOTICE 1, DOD MIL-STD-2407]
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- 2004-03-31
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References to the Defense Mapping Agency and the acronym DMA within the text of the document will be updated to the National Geospatial-Intelligence Agency and NGA respectively; the next time the document is technically updated.
GRIDDED INSTALLATION PHOTOGRAPH (GIP)
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- 49.100
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- 2004-03-31
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MIL-N-89404 remains inactive for new design (see NOTICE 1).
NON-SIOP OPTION (NSO) SUPPORT
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- 2004-03-31
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Describes the procedure for the assessment of medical devices and their constituent materials with regard to their potential to produce irritation and delayed-type hypersensitivity. It includes pretest considerations, details of the test procedures, and key factors for the interpretation of the results.
Biological evaluation of medical devices Part 10: Tests for irritation and delayed-type hypersensitivity
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- 11.100
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- 2004-03-05
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In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials.
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- 07.100.10
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- 2004-01-01
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- 2004-01-05
Appareils industriels, scientifiques et médicaux (ISM) ?fréquence radioélectrique Caractéristiques de perturbations électromagnétiques Limites et méthodes de mesure Premiere Edition; CEI CISPR 11:2003
Industrial, scientific and medical (ISM) devices radio frequency Electromagnetic disturbance characteristics Limits and measurement methods Premiere Edition; IEC CISPR 11:2003
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- 2004-01-01
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Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects.
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- 11.100.10
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- 2003-10-01
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- 2003-10-20
This part of ISO 10993 describes a) the general principles governing the biological evaluation of medical devices; b) the categorization of devices based on the nature and duration of their contact with the body; c) the selection of appropriate tests. This part of ISO 10993 does not cover testing of materials and devices that do not come into direct or indirect contact with the patient's body, nor does it cover biological hazards arising from any mechanical failure. NOTE Other parts of ISO 10993 cover specific tests (see also the rationale in A.2).
Biological evaluation of medical devices Part 1: Evaluation and testing ISO 10993-1:2003
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- 11.100.20
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- 2003-08-01
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Medical electrical equipment ?Part 1-2: General requirements for safety ?Collateral standard: Electromagnetic compatibility ?Requirements and tests Edition 2.1; IEC 60601-1-2: 2004; Amendment 1: 2006
Medical electrical equipment ?Part 1-2: General requirements for safety ?Collateral standard: Electromagnetic compatibility ?Requirements and tests Edition 2.1; IEC 60601-1-2: 2004; Amendment 1: 2006
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- 2003-06-01
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INTEROPERABILITY STANDARD FOR THE JOINT RANGE EXTENSION APPLICATION PROTOCOL (JREAP)
INTEROPERABILITY STANDARD FOR THE JOINT RANGE EXTENSION APPLICATION PROTOCOL (JREAP)
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- 2002-09-30
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Stability testing of in vitro diagnostic reagents.
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- 11.100.10
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- 2002-08-01
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- 2002-08-05
This standard defines the requirements for bar coding of geospatial products.
BAR CODING FOR GEOSPATIAL PRODUCTS
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- 2002-08-01
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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
Medical electrical equipment ?Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment Second Edition; IEC 60601-2-34:2000
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- 2002-06-01
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Medical electrical equipment - Part 2-23
Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment Second Edition
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- 2002-06-01
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The Canadian Standards Association, which operates under the name CSA International (CSA), under whose auspices this National Standard has been produced, was chartered in 191 9 and accredited by the Standards Council of Canada to the National Standar
Medical Electrical Equipment - Part 1-4: General Requirements for Safety - Collateral Standard: Programmable Electrical Medical Systems First Edition
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- 2002-04-01
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Further information on IEC publications
Medical Electrical Equipment - Part 1-1: General Requirements for Safety - Collateral Standard: Safety Requirements for Medical Electrical Systems Second Edition [Superseded: CSA C22.2 NO 114-M90-CAN/CSA]
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- 2002-04-01
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INTEROPERABILITY AND PERFORMANCE STANDARD FOR THE DATA CONTROL WAVEFORM
INTEROPERABILITY AND PERFORMANCE STANDARD FOR THE DATA CONTROL WAVEFORM
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- 发布
- 2002
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RASTER PRODUCT FORMAT
RASTER PRODUCT FORMAT
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- 2001-08-16
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This document is a companion document to the military standard for Raster Product Format (RPF) , MIL-STD-2411. It contains all registered data values referenced in the standard.
REGISTERED DATA VALUES FOR RASTER PRODUCT FORMAT
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- 2001-08-16
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Medical Electrical Equipment - Part 2-24: Particular Requirements for the Safety of Infusion Pumps and Controllers First Edition; IEC 60601-2-24:1998
Medical Electrical Equipment - Part 2-24: Particular Requirements for the Safety of Infusion Pumps and Controllers First Edition
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- 2001-06-01
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