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USGBC HOMES REF GUIDE - LEED for Homes REFERENCE GUIDE
January 1, 2009 - USGBC

LEED for Homes Overview and Process LEED for Homes is a national, voluntary certification system, developed by national experts and experienced builders, that promotes the design and construction of high-performance green homes and encourages the adoption of sustainable...

USGBC HOMES RATING SYS - LEED for Homes Rating System
January 1, 2008 - USGBC

General Clarification: LEED for Homes cannot be offered outside of the US at this time because of the technical limitations of adapting the rating system to local codes and the logistical limitations of providing a uniform international verification network. This decision will be revisited...

DOD I 6490.15 - Integration of Behavioral Health Personnel (BHP) Services Into Patient-Centered Medical Home (PCMH) Primary Care and Other Primary Care Service Settings
October 23, 2014 - NPFC

PURPOSE. In accordance with the authority in DoD Directive 5124.02 (Reference (a)), this instruction: a. Establishes policy, assigns responsibilities, and prescribes procedures for attainment of inter-Service standards for developing, initiating, and maintaining adult behavioral health services in...

JIS MEDICAL DEVICES II - JIS Medical Devices II Handbook
January 1, 2015 - JSA
A description is not available for this item.
JIS MEDICAL DEVICES IV - JIS Medical Devices IV Handbook
January 1, 2015 - JSA
A description is not available for this item.
JIS MEDICAL DEVICES I - JIS Medical Devices I Handbook
January 1, 2015 - JSA
A description is not available for this item.
JIS MEDICAL DEVICES III - JIS Medical Devices III Handbook
January 1, 2015 - JSA
A description is not available for this item.
DS/EN 16777 - Chemical disinfectants and antiseptics – Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area – Test method and requirements (phase 2/step 2)
December 17, 2018 - DS

This document specifies a test method and the minimum requirements for virucidal activity of chemical disinfectants that form a homogeneous physically stable preparation when diluted with hard water - or in the case of ready-to-use products - with water. This document applies to products that are...

DS/EN 17126 - Chemical disinfectants and antiseptics – Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area – Test method and requirements (phase 2, step 1)
December 10, 2018 - DS

This document specifies a test method and the minimum requirements for sporicidal activity of chemical disinfectant that form a homogeneous, physically stable preparation when diluted with hard water, or - in the case of ready-to-use products - with water. Products can only be tested at a...

DS/EN 17111 - Chemical disinfectants and antiseptics – Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area – Test method and requirements (phase 2, step 2)
November 5, 2018 - DS

This document specifies a test method and the minimum requirements for virucidal activity of chemical disinfectant products that form a homogeneous, physically stable preparation when diluted with hard water - or in the case of ready-to-use products - with water. This document applies to products...

IEC 61010-2-101 - Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
October 1, 2018 - IEC

Equipment included in scope This part of IEC 61010 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in...

IEC 61010-2-101 REDLINE - Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
October 1, 2018 - IEC

Equipment included in scope This part of IEC 61010 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in...

DS/ISO/TR 21954 - Guidance on the selection of the appropriate means of ventilation based on the intended patient, use environment, and operator
October 3, 2018 - DS

This document considers and identifies criteria about the intended PATIENT population, intended USE ENVIRONMENT, and intended OPERATOR across the spectrum of the types of ventilation-related equipment as listed below: -- gas-powered resuscitator as specified in ISO 10651-5 [1] 2; --...

IEC 60335-2-8 - Household and similar electrical appliances – Safety – Part 2-8: Particular requirements for shavers, hair clippers and similar appliances
November 1, 2018 - IEC

This clause of Part 1 is replaced by the following. Battery-operated appliances and other d.c. supplied appliances are within the scope of this standard. Dual supply appliances, either mains-supplied or battery-operated, are regarded as battery-operated appliances when operated in the battery mode...

CSA Z314 - Canadian medical device reprocessing
January 1, 2018 - CSA

This Standard is intended to address the safe, effective, and reliable reprocessing of reusable medical devices at each phase of the reprocessing workflow, including a) establishing a QMS for the MDRD, including i) key performance indicators; ii) policies and procedures; iii) documentation;...

IEC 60335-2-15 - Household and similar electrical appliances - Safety - Part 2-15: Particular requirements for appliances for heating liquids
November 1, 2018 - IEC

This clause of Part 1 is replaced by the following This International Standard deals with the safety of electrical appliances for heating liquids for household and similar purposes, their rated voltage being not more than 250 V. NOTE 101 Some appliances can be used for heating food. NOTE 102...

ISO DIS 80601-2-12 - Medical electrical equipment - Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
August 6, 2018 - ISO

This document applies to the basic safety and essential performance of a ventilator in combination with its accessories, hereafter referred to as me equipment: - intended for use in an environment that provides specialized care for patients whose conditions can be life-threatening and who can...

DS/ISO 80601-2-79 - Medical electrical equipment – Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
July 23, 2018 - DS

This document applies to the basic safety and essential performance of ventilatory support equipment, as defined in 201.3.205, for ventilatory impairment, as defined in 201.3.202, hereafter also referred to as me equipment, in combination with its accessories: - intended for use in the home...

DS/ISO 80601-2-80 - Medical electrical equipment – Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
July 23, 2018 - DS

This document applies to the basic safety and essential performance of ventilatory support equipment, as defined in 201.3.205, for ventilatory insufficiency, as defined in 201.3.204, hereafter also referred to as me equipment, in combination with its accessories: - intended for use in the...

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