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JSA - JIS T 1004 - TESTING METHODS FOR MECHANICAL SAFETY OF MEDICAL ELECTRICAL EQUIPMENT Organization: JSA
NBN - EN 14350-1 - CHILD USE AND CARE ARTICLES - DRINKING EQUIPMENT - PART 1: GENERAL AND MECHANICAL REQUIREMENTS AND TESTS Organization: NBN
Date: 2004-09-30
Description: It does not apply to drinking equipment designed for medical applications or for use under medical supervision.This document is not applicable to soothers.
NBN - EN 14350-1 - CHILD USE AND CARE ARTICLES - DRINKING EQUIPMENT - PART 1: GENERAL AND MECHANICAL REQUIREMENTS AND TESTS Organization: NBN
Date: 2004-09-30
Description: It does not apply to drinking equipment designed for medical applications or for use under medical supervision.This document is not applicable to soothers.
ASTM - 13.02 - MEDICAL AND SURGICAL MATERIALS AND DEVICES (II): F2502-LATEST; EMERGENCY MEDICAL SERVICES; SEARCH AND RESCUE; ANESTHETIC AND RESPIRATORY EQUIPMENT - TO PURCHASE CALL 1-800-854-7179 USA/CANADA OR 303-397-7956 WORLDWIDE Organization: ASTM
Date: 2016-09-01
Description: Each standard typically covers manufacture, chemical requirements, mechanical requirements, special tests, and certification. Topics in Volume 13.02 also include: Emergency Medical Services -covers emergency medical dispatch, ambulances, fixed wing basic and specialized units, and basic training for emergency medical technicians.
ASSE SERIES 6000 - PROFESSIONAL QUALIFICATIONS STANDARD FOR MEDICAL GAS SYSTEMS PERSONNEL – MEDICAL GAS SYSTEMS GENERALISTS – MEDICAL GAS SYSTEMS INSTALLERS – BULK MEDICAL GAS SYSTEMS INSTALLERS – MEDICAL GAS SYSTEMS INSPECTORS – MEDICAL GAS SYSTEMS VERIFIERS – BULK MEDICAL GAS SYSTEMS VERIFIERS – MEDICAL GAS SYSTEMS MAINTENANCE PERSONNEL – MEDICAL GAS SYSTEMS INSTRUCTORS – BULK MEDICAL GAS SYSTEMS INSTRUCTORS Organization: ASSE
Date: 2015-07-01
Description: In subsequent revisions, requirements for medical gas generalists, bulk medical gas systems installers, bulk medical gas systems verifiers, and bulk medical gas systems instructors were added.
CSA SPE-3000 - MODEL CODE FOR THE FIELD EVALUATION OF MEDICAL ELECTRICAL EQUIPMENT AND SYSTEMS - FIRST EDITION; ERRATA: JUNE 2016 Organization: CSA
Date: 2015-01-01
Description: This Model Code applies to the safety of medical electrical equipment (MEE) and medical electrical systems (MES) as it pertains to safety from electrical shock and fire and mechanical hazards.
AAMI HE74 - HUMAN FACTORS DESIGN PROCESS FOR MEDICAL DEVICES Organization: AAMI
Date: 2001-01-01
Description: ., human factors engineers, industrial designers, technical writers, information designers, software developers, mechanical engineers, electrical engineers, packaging engineers); c) Medical researchers and other interested clinicians; and d) Marketers and other business professionals in the medical device industry.
IEC 61223-3-1 - EVALUATION AND ROUTINE TESTING IN MEDICAL IMAGING DEPARTMENTS - PART 3-1: ACCEPTANCE TESTS - IMAGING PERFORMANCE OF X-RAY EQUIPMENT FOR RADIOGRAPHIC AND RADIOSCOPIC SYSTEMS - EDITION 1.0 Organization: IEC
Date: 1999-03-01
Description: This standard applies to the performance of X-RAY EQUIPMENT in the ACCEPTANCE TEST on the following medical diagnostic X-RAY EQUIPMENT and ASSOCIATED EQUIPMENT: – radiography equipment, for example: • stationary radiography EQUIPMENT; • mobile radiography EQUIPMENT; • skull radiography EQUIPMENT; • lung radiography EQUIPMENT; • TOMOGRAPHY EQUIPMENT – excluding COMPUTED TOMOGRAPHY; • radiography devices (SPOTFILM DEVICES) in RADIOSCOPY EQUIPMENT; • angiography EQUIPMENT (excluding DSA function); • CINERADIOGRAPHY equipment; – RADIOSCOPY EQUIPMENT, including: • combined radiographic and radioscopic EQUIPMENT.
DS/EN 61965 - MECHANICAL SAFETY OF CATHODE RAY TUBES Organization: DS
Date: 2003-11-12
Description: These requirements apply to CRTs intended for use in apparatus including electrical and electronic measuring and testing equipment, information technology equipment, medical equipment, telephone equipment, television equipment and other similar electronic apparatus.
IEC 61965 - MECHANICAL SAFETY OF CATHODE RAY TUBES - EDITION 2.0 Organization: IEC
Date: 2003-07-01
Description: These requirements apply to CRTs intended for use in apparatus including electrical and electronic measuring and testing equipment, information technology equipment, medical equipment, telephone equipment, television equipment and other similar electronic apparatus.
CSA E61965 - MECHANICAL SAFETY OF CATHODE RAY TUBES - SECOND EDITION Organization: CSA
Date: 2004-04-01
Description: These requirements apply to CRTs intended for use in apparatus including electrical and electronic measuring and testing equipment, information technology equipment, medical equipment, telephone equipment, television equipment and other similar electronic apparatus.
ASTM F2150 - STANDARD GUIDE FOR CHARACTERIZATION AND TESTING OF BIOMATERIAL SCAFFOLDS USED IN TISSUE-ENGINEERED MEDICAL PRODUCTS Organization: ASTM
Date: 2013-10-01
Description: This guide is a resource of currently available test methods for the characterization of the compositional and structural aspects of biomaterial scaffolds used to develop and manufacture tissue-engineered medical products (TEMPs). The test methods contained herein guide characterization of the bulk physical, chemical, mechanical, and surface properties of a scaffold construct.
CSA ISO 16571 - SYSTEMS FOR EVACUATION OF PLUME GENERATED BY MEDICAL DEVICES - FIRST EDITION Organization: CSA
Date: 2016-01-01
Description: This International Standard specifies requirements and guidelines for the design, manufacture, installation, function, performance, maintenance, servicing, documentation, testing, and commissioning of equipment for evacuation of plume generated by medical devices.
UL 61965 - UL STANDARD FOR SAFETY MECHANICAL SAFETY FOR CATHODE RAY TUBES - SECOND EDITION; REPRINT WITH REVISIONS THROUGH AND INCLUDING MARCH 24, 2014 Organization: UL
Date: 2004-07-27
Description: These requirements apply to CRTs intended for use in apparatus including electrical and electronic measuring and testing equipment, information technology equipment, medical equipment, telephone equipment, television equipment and other similar electronic apparatus.
DSF/FPREN 62638 - RECURRENT TEST AND TEST AFTER REPAIR OF ELECTRICAL EQUIPMENT Organization: DS
Description: . - electric tools - electric heating devices - electric motor devices - lighting fixtures, which are not part of the fixed installation - devices for the entertainment, information and communication technology - extension cords, multi-way adapters and connection leads This standard does not apply - To the verification of the electrical installation which is covered by IEC 60364-6 - to equipment, for which special legislation, regulations and standards should be noted for corrective MAINTENANCEand/or verifications (for example devices for EX-zones or for mining) - to medical ELECTRICAL EQUIPMENT according to IEC 60601-1 (see also IEC 62353) - to arc welding equipment according to IEC 60974-1 (see IEC 60974-4) - to protective devices for household and similar use.
VA 27 11 00 - COMMUNICATIONS EQUIPMENT ROOM FITTINGS Organization: VA
Date: 2006-10-01
Description: This Section specifies the furnishing, installing, certification, testing, and guaranty of a complete and operating Voice and Digital Cable Distribution System (here-in-after referred to as "the System"), and associated equipment and hardware to be installed in the VA //Medical Center//, //, Out Patient Clinic// //, Nursing Home Care Unit// //, Domiciliary// //, or____________________// here-in-after referred to as "the Facility".
DS/EN 62359 - ULTRASONICS - FIELD CHARACTERIZATION - TEST METHODS FOR THE DETERMINATION OF THERMAL AND MECHANICAL INDICES RELATED TO MEDICAL DIAGNOSTIC ULTRASONIC FIELDS Organization: DS
Date: 2011-03-18
Description: Major changes with respect to the previous edition include the following: - The methods of determination set out in the first edition of this standard were based on those contained in the American standard for Real-Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment (ODS) and were intended to yield identical results.
VA 27 31 00 - VOICE COMMUNICATIONS SWITCHING AND ROUTING EQUIPMENT Organization: VA
Date: 2006-10-01
Description: This section specifies the furnishing, installing, certification, testing, and guaranty of a complete and operating Telephone Electronic Private Branch Exchange (EPBX) equipment and interconnecting cable (not cable distribution plant) system (here-in-after referred to as "the System"), and associated equipment to be installed in the VA //Medical Center//, //, Out Patient Clinic// //, Nursing Home Care Unit// //, Domiciliary// //, or ____________________// here-in-after referred to as "the Facility".\ The System shall include, but not be limited to, telephone processing switch, equipment cabinets, interface enclosures, and relay racks, stand-by battery(s), necessary combiners, traps, and filters; interconnection nodes and/or amplifiers; telephone instruments; auxiliary systems; and necessary passive devices such as: protectors, isolators, splitters, couplers, cable "patch", "punch down", and cross-connector blocks or devices, cable management items, voice and digital cable distribution system, and associated hardware.
VA 27 31 31 - VOICE COMMUNICATIONS SWITCHING AND ROUTING EQUIPMENT - EXTENSION Organization: VA
Date: 2006-10-01
Description: This section specifies the furnishing, installing, certification, testing, and guaranty of a complete and operating extension of an existing operating Telephone System, and associated equipment (here-inafter referred to as "the System") and associated equipment to be installed in the VA // Medical Center //, //, Out Patient Clinic // //, Nursing Home Care Unit // //, Domiciliary// //, or here-in-after referred to as "the Facility".
ASTM F2883 - STANDARD GUIDE FOR CHARACTERIZATION OF CERAMIC AND MINERAL BASED SCAFFOLDS USED FOR TISSUE-ENGINEERED MEDICAL PRODUCTS (TEMPS) AND AS DEVICE FOR SURGICAL IMPLANT APPLICATIONS Organization: ASTM
Date: 2011-12-01
Description: This guidance document covers the chemical, physical, biological, and mechanical characterization requirements for biocompatible mineral- and ceramic-based scaffolds used solely as device or to manufacture tissue-engineered medical products (TEMPs). In this guide, the pure device or the TEMPs product will be referred to as scaffold.

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