Accuris Datasheets for Standards and Technical Documents
Standards and technical documents includes standards, codes, regulation, handbooks, manuals, comprehensive guides and other formal publications. Standards, codes, and regulation establish uniform specifications, procedures or technical criteria.
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| Product Name | Notes |
|---|---|
| (RESTRICTED) AEROMEDICAL ASPECTS OF AIRCRAFT ACCIDENT AND INCIDENT INVESTIGATION | |
| (RESTRICTED) AIRCRAFT CABIN PRESSURIZING TEST CONNECTIONS | |
| (RESTRICTED) APERTURE OF TERMINAL RING OR LINK OF AIRCRAFT LIFTING SLINGS | |
| (RESTRICTED) DOCTRINE OTAN DE L\x92APPUI-FEU | |
| (RESTRICTED) ESSAIS D\x92\xc9VALUATION DE LA S\xc9CURIT\xc9 ET DE L\x92APTITUDE AU SERVICE (S3) DES MUNITIONS TIR\xc9ES \xc0 L\x92\xc9PAULE | |
| (RESTRICTED) ESSAIS D\x92\xc9VALUATION DE LA S\xc9CURIT\xc9 ET DE L\x92APTITUDE AU SERVICE DES MUNITIONS DE CALIBRE INF\xc9RIEUR \xc0 20 mm | |
| (RESTRICTED) EXPLOSIVES SAFETY RISK ANALYSIS - GUIDELINES FOR RISK-BASED DECISIONS | |
| (RESTRICTED) EXPLOSIVES SAFETY RISK ANALYSIS - TECHNICAL BACKGROUND | |
| (RESTRICTED) NATO ASSET TRACKING "TO BE" BUSINESS PROCESS MODEL | |
| (RESTRICTED) NATO GLOSSARY OF IDENTIFICATION, ENGLISH AND FRENCH | |
| (RESTRICTED) NATO GUIDELINES FOR THE STORAGE, MAINTENANCE AND TRANSPORT OF AMMUNITION ON DEPLOYED MISSIONS OR OPERATIONS | |
| (RESTRICTED) NATO INDIRECT FIRES AUTOMATIC DATA PROCESSING (ADP) SYSTEM INTEROPERABILITY | |
| (RESTRICTED) RACCORDS DE CONDITIONNEMENT D'AIR | |
| (RESTRICTED) SAFETY AND SUITABILITY FOR SERVICE ASSESSMENT TESTING FOR AIRCRAFT LAUNCHED MUNITIONS | |
| (RESTRICTED) SAFETY AND SUITABILITY FOR SERVICE ASSESSMENT TESTING FOR SURFACE AND UNDERWATER LAUNCHED MUNITIONS | |
| (RESTRICTED) SAFETY AND SUITABILITY FOR SERVICE ASSESSMENT TESTING OF LARGE CALIBER AMMUNITION GREATER THAN 40MM | |
| (RESTRICTED) USERS HANDBOOK AND GUIDE TO CAPS | |
| AASHTO Guide specifications for LRFD Seismic Bridge Design | |
| AASHTO LRFD Bridge Design Guide Specifications for GFRP-Reinforced Concrete Bridge Decks and Traffic Railings | |
| AATCC Style Guide for Writing Test Methods | |
| AATCC Technical Manual Mid-Year Supplement 2020 | |
| Active implantable medical devices\x97Electroma gnetic compatibility\x97EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices | |
| ADVANCES IN ADDITIVE MANUFACTURING WITH POWDER METALLURGY | |
| ADVICE ON THE DEVELOPMENT OF THE IMPLEMENTATION PARAGRAPH FOR INCLUSION WITHIN STANAGS | |
| AEROMEDICAL TRAINING OF AIRCREW IN AIRCREW CBRN EQUIPMENT AND PROCEDURES | |
| AIRCRAFT FITTING FOR PRESSURE REPLENISHMENT OF GAS TURBINE ENGINES WITH OIL | |
| AIRCRAFT JACKING | |
| AIRCRAFT TOWING ATTACHMENTS AND DEVICES | |
| ALLIED JOINT DOCTRINE DEVELOPMENT | |
| Aluminum Automotive Recycling Guidelines | |
| Application of risk management for IT Networks incorporating medical devices \x97 Part 1: Roles, responsibilities and activities | |
| Application of risk management for IT networks incorporating medical devices-Part 2-8: Application guidance-Guidance on standards for establishing the security capabilities identified in IEC 80001-2-2 | |
| Application of risk management for IT-networks incorporating medical devices - Part 2-1: Step by step risk management of medical IT-networks; Practical applications and examples | |
| Application of risk management for IT-networks incorporating medical devices - Part 2-2: Guidance for the disclosure and communication of medical device security needs, risks and controls | |
| Application of risk management for IT-networks incorporating medical devices - Part 2-3: Guidance for Wireless Networks | |
| Application of risk management for IT-networks incorporating medical devices - Part 2-4: General implementation guidance for healthcare delivery organizations | |
| Application of risk management for ITnetworks incorporating medical - Application guidance - Part 2-6: Guidance for responsibility agreements | |
| Application of risk management for ITnetworks incorporating medical - Application guidance - Part 2-7: Guidance for Healthcare Delivery Organizations (HDOs) on how to selfassess their conformance with IEC 80001-1 | |
| Application of risk management for ITnetworks incorporating medical devices \x96 Part 2-5: Application guidance \x96 Guidance on distributed alarm systems | |
| ARTILLERY PROCEDURES FOR ATOMATIC DATA PROCESSING (ADP) SYSTEM INTEROPERABILITY | |
| Aseptic processing of health care products - Part 3: Lyophilization | |
| Aseptic processing of health care products - Part 4: Clean-in-place technologies | |
| Aseptic processing of health care products - Part 5: Sterilization in place | |
| Aseptic processing of health care products - Part 6: Isolator systems | |
| Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products | |
| Aseptic processing of health care products-Part 2: Sterilizing filtration | |
| Aseptic processing of health care products\x97 Part 1: General requirements | |
| Assessment of the impact of the most significant changes in Amendment 1 to IEC 60601-1:2005 and mapping of the clauses of IEC 60601-1:2005 to the previous edition | |
| Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device | |
| Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization | |
| Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | |
| Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys | |
| Biological evaluation of medical devices - Part 17: Methods for the establishment of allowable limits for leachable substances | |
| Biological evaluation of medical devices - Part 2: Animal welfare requirements | |
| Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products | |
| Biological evaluation of medical devices-Guidance on the conduct of biological evaluation within a risk management process | |
| Biological evaluation of medical devices-Part 6: Tests for local effects after implantation | |
| Biological evaluation of medical devices-Part 7: Ethylene oxide sterilization residuals | |
| Biological evaluation of medical devices\x97 Part 20: Principles and methods for immunotoxicology testing of medical devices | |
| Biological evaluation of medical devices\x97Part 11: Tests for systemic toxicity | |
| Biological evaluation of medical devices\x97Part 13: Identification and quantification of degradation products from polymeric devices | |
| Biological evaluation of medical devices\x97Part 14: Identification and quantification of degradation products from ceramics | |
| Biological evaluation of medical devices\x97Part 16: Toxicokinetic study design for degradation products and leachables | |
| Biological evaluation of medical devices\x97Part 19: Physico-chemical, morphological and topographical characterization of materials | |
| Biological evaluation of medical devices\x97Part 1: Evaluation and testing within a risk management process | |
| Biological evaluation of medical devices\x97Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | |
| Biological evaluation of medical devices\x97Part 4: Selection of tests for interactions with blood | |
| Biological evaluation of medical devices\x97Part 5: Tests for in vitro cytotoxicity | |
| BOOKCASE, STEEL, UNITIZED | |
| CADRE DE GESTION DES PROGRAMMES OTAN (mod\xe8le de cycle de vie OTAN) | |
| Cardiac rhythm management devices \x97 Symbols to be used with cardiac rhythm management device labels, and information to be supplied \x97 General requirements | |
| Cardiovascular biological evaluation of medical devices - Guidance for absorbable implants | |
| Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses | |
| Cardiovascular implants - Endovascular devices - Part 2: Vascular stents | |
| Cardiovascular implants \x97 Endovascular devices \x97 Part 3: Vena cava filters | |
| Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) | |
| Cardiovascular implants and artificial organs - Checklist for preoperative extracorporeal circulation equipment setup | |
| Cardiovascular implants and artificial organs - Hard-shell cardiotomy/ venous reservoir systems (with/without filter) and soft venous reservoir bags | |
| Cardiovascular implants and artificial organs-Cardiopulmona ry bypass systems-Arterial blood line filters | |
| Cardiovascular implants and artificial organs-Requirements for singleuse tubing packs for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO) | |
| Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems | |
| Cardiovascular implants and extracorporeal systems-Cardiopulmon ary bypass systems-Venous bubble traps | |
| Cardiovascular implants and extracorporeal systems-Centrifugal blood pumps | |
| Cardiovascular implants\x97Cardiac valve prostheses\x97Part 1: General requirements | |
| Cardiovascular implants\x97Cardiac valve prostheses\x97Part 2: Surgically implanted heart valve substitutes | |
| Cardiovascular implants\x97Cardiac valve prostheses\x97Part 3: Heart valve substitutes implanted by transcatheter techniques | |
| Cardiovascular implants\x97Tubular vascular prostheses | |
| CHAIRS, WOOD, GENERAL OFFICE | |
| Clinical investigation of medical devices for human subjects\x97Good clinical practice | |
| Considerations of unaddressed safety aspects in the second edition of IEC 60601-1 and proposals for new requirements | |
| CORRESPONDANCE MILITAIRE | |
| CREDENZA, OFFICE, STEEL | |
| Desktop Publishing Standards for Allied Publications | |
| Evaluation of CPB devices relative to their capabilities of reducing the transmission of gaseous microemboli (GME) to a patient during cardiopulmonary bypass | |
| EXPLOSIVES SAFETY RISK ANALYSIS PART I: GUIDELINES FOR RISK-BASED DECISIONS | |
| Extracorporeal systems for blood purification\x97Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators | |
| Extracorporeal systems for blood purification\x97Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters | |
| Extracorporeal systems for blood purification\x97Part 3: Plasmafilters | |
| FACILITATING THE DEVELOPMENT AND USE OF CIVIL STANDARDS | |
| FIL T\xc9MOIN (\xc0 CASSER) POUR LE BLOCAGE DE S\xc9CURIT\xc9 DES COMMANDES ET MAT\xc9RIELS SUR A\xc9RONEFS | |
| FLAMMES DE SIGNALISATION | |
| General testing procedures for medical electrical equipment | |
| Glossary of Abbreviations Used in NATO Documents | |
| Graphical symbols for electrical equipment in medical practice | |
| Guidance for uncertainty analysis regarding the application of ISO/TS 10974 | |
| GUIDE TO OBTAINING AIR-TO-AIR REFUELLING CLEARANCES AND COMPATIBILITY CERTIFICATION | |
| High frequency surgical equipment \x96 Operation and maintenance | |
| Implants for surgery - Active implantable medical devices - Part 1: General requirements for safety, marking and for information to be provided by the manufacturer | |
| Implants for surgery - Active implantable medical devices - Part 3: Implantable neurostimulators | |
| Implants for surgery\x97Active implantable medical devices\x97Part 4: Implantable infusion pumps | |
| INITIAL INVESTIGATION AND IMMEDIATE MANAGEMENT OF LASER EYE DAMAGE IN AIRCREW | |
| LOW PRESSURE AIR AND ASSOCIATED ELECTRICAL CONNECTIONS FOR AIRCRAFT ENGINE STARTING | |
| MANPOWER POLICY AND PROCEDURES | |
| MANUAL FOR THE DEVELOPMENT OF AN EXPLOSIVES SAFETY SITE PLAN BASED ON AASTP-1 | |
| MANUAL OF NATO SAFETY PRINCIPLES FOR THE STORAGE OF MILITARY AMMUNITION AND EXPLOSIVES | |
| MANUAL ON EXPLOSIVES SAFETY RISK ANALYSIS | |
| MANUEL DE TERMINOLOGIE DE L\x92OTAN | |
| Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software | |
| Medical device software - Part 2: Validation of software for medical device quality systems | |
| Medical device software - Part 3: Process reference model of medical device software life cycle processes | |
| Medical device software - Software life cycle processes | |
| Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents | |
| Medical devices utilizing animal tissues and their derivatives - Part 4: Principles for elimination and/or inactivation of transmissible spongiform encephalopathy (TSE) agents and validation assays for those processes | |
| Medical devices utilizing animal tissues and their derivatives-Part 1: Application of risk management | |
| Medical devices utilizing animal tissues and their derivatives-Part 2: Controls on sourcing, collection and handling | |
| Medical devices\x97 Application of risk management to medical devices | |
| Medical devices\x97 Guidance on the application of ISO 14971 | |
| Medical devices\x97 Post-market surveillance for manufacturers | |
| Medical devices\x97Informati on to be supplied by the manufacturer | |
| Medical devices\x97Part 1: Application of usability engineering to medical devices | |
| Medical devices\x97Part 2: Guidance on the application of usability engineering to medical devices | |
| Medical devices\x97Quality management systems\x97Requireme nts for regulatory purposes | |
| Medical devices\x97Symbols to be used with information to be supplied by the manufacturer\x97 Part 1: General requirements | |
| Medical devices\x97Symbols to be used with medical device labels, labeling, and information to be supplied\x97 Part 2: Symbol development, selection and validation | |
| Medical Electrical Equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators | |
| Medical Electrical Equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators | |
| Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers | |
| Medical electrical equipment - Part 2-25: Particular requirements for the basic safety and essential performance of electrocardiographs | |
| Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment | |
| Medical electrical equipment - Part 2-47: Particular requirements for the basic safety and essential performance of ambulatory electrocardiographic systems | |
| Medical Electrical Equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment | |
| Medical electrical equipment-Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories | |
| Medical electrical equipment-Part 2-30: Particular requirements for basic safety and essential performance of automated type non-invasive sphygmomanometers | |
| Medical electrical equipment\x97Part 1-12: General requirements for basic safety and essential performance\x97 Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical... | |
| Medical electrical equipment\x97Part 1-2: General requirements for basic safety and essential performance\x97 Collateral standard: Electromagnetic disturbances\x97Requ irements and tests | |
| Medical electrical equipment\x97Part 1-8: General requirements for basic safety and essential performance\x97Colla teral standard: General requirements, test and guidance for alarm systems in medical electrical equipment and medical electrical systems... | |
| Medical electrical equipment\x97Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment | |
| Medical electrical equipment\x97Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment | |
| Medical electrical equipment\x97Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery | |
| Medical electrical equipment\x97Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment | |
| Medical electrical equipment\x97Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation | |
| Medical products containing viable human cells - Application of risk management and requirements for processing practices | |
| NATO Glossary of Abbreviations Used in NATO Documents and Publications | |
| NATO GLOSSARY OF TERMS AND DEFINITIONS (ENGLISH AND FRENCH) | |
| NATO GUIDELINES FOR THE STORAGE, MAINTENANCE AND TRANSPORT OF AMMUNITION ON DEPLOYED MISSIONS OR OPERATIONS | |
| NATO STANDARD BAR CODE HANDBOOK | |
| NATO SYSTEM LIFE CYCLE PROCESSES | |
| Non-invasive sphygmomanometers - Part 1: Requirements and test methods for nonautomated measurement type | |
| Non-invasive sphygmomanometers - Part 2: Clinical investigation of intermittent automated measurement type | |
| OFFICE FURNITURE, BOOKCASE, WOOD, UNITIZED (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE, CABINET, TELEPHONE, EXECUTIVE, WOOD AND METAL | |
| OFFICE FURNITURE, CREDENZA, WOOD, UNITIZED (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE, CREDENZAS, EXECUTIVE, WOOD AND METAL | |
| OFFICE FURNITURE, DESK ATTACHMENTS, L-UNIT TABLES, STEEL, UNITIZED | |
| OFFICE FURNITURE, DESK, DESK ATTACHMENTS, EXECUTIVE, WOOD AND METAL | |
| OFFICE FURNITURE, DESKS, L-UNIT, STEEL, UNITIZED | |
| OFFICE FURNITURE, EXECUTIVE (COMBINATION METAL AND WOOD) | |
| OFFICE FURNITURE, EXECUTIVE, COMBINATION METAL AND WOOD CHAIRS, STRAIGHT, CHAIRS, ROTARY | |
| OFFICE FURNITURE, EXECUTIVE, COMBINATION METAL AND WOOD; DAVENPORT AND CHAIR, LOUNGE, EASY | |
| OFFICE FURNITURE, EXECUTIVE, COMBINATION METAL AND WOOD; SETTEE, SECTIONAL UNIT (WITHOUT ARMS) | |
| OFFICE FURNITURE, STEEL, SECTIONAL | |
| OFFICE FURNITURE, STEEL, UNITIZED, GENERAL SPECIFICATION | |
| OFFICE FURNITURE, TABLE, EXECUTIVE, WOOD AND METAL | |
| OFFICE FURNITURE, TABLES, WOOD, UNITIZED (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE, TOP ASSEMBLY, DESK, AND SUPPORT PANELS, STEEL, UNITIZED | |
| OFFICE FURNITURE, WOOD, UNITIZED (GENERAL SPECIFICAION) | |
| OFFICE FURNITURE: BOOKCASES, EXECUTIVE TYPE, WOOD, TRADITIONAL, (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: CABINET, TELEPHONE, EXECUTIVE TYPE, WOOD TRADITIONAL (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: COSTUMER, EXECUTIVE TYPE, WOOD, TRADITIONAL (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: COSTUMER, EXECUTIVE TYPE, WOOD, TRADITIONAL | |
| OFFICE FURNITURE: CREDENZA, EXECUTIVE OFFICE, WOOD, TRADITIONAL (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: DESK, EXECUTIVE TYPE, WOOD, TRADITIONAL (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: DESKS, DESK ATTACHMENTS, WOOD, UNITIZED (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: EXECUTIVE, CONTEMPORARY FULL PANEL | |
| OFFICE FURNITURE: EXECUTIVE, CONTEMPORARY, FULL PANEL | |
| OFFICE FURNITURE: SOFA; CHAIR, EASY, EXECUTIVE, TRADITIONAL | |
| OFFICE FURNITURE: STORAGE UNITS, WOOD, UNITIZED (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: TABLES, EXECUTIVE TYPE, WOOD, TRADITIONAL (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: TYPEWRITER STAND, EXECUTIVE OFFICE, WOOD, TRADITIONAL (DETAILED SPECIFICATION) | |
| OFFICE FURNITURE: TYPEWRITER STAND, WOOD, UNITIZED | |
| Packaging for terminally sterilized medical devices \x96 Part 2: Validation requirements for forming, sealing, and assembly processes | |
| Packaging for terminally sterilized medical devices\x97 Guidance on the application of ISO 11607-1 and ISO 11607-2 | |
| Packaging for terminally sterilized medical devices\x97 Part 1: Requirements for materials, sterile barrier systems, and packaging | |
| Packaging for terminally sterilized medical devices\x97Part 1: Requirements for materials, sterile barrier systems and packaging systems Amendment 1: Application of risk management | |
| Packaging for terminally sterilized medical devices\x97Part 2: Validation requirements for forming, sealing and assembly processes Amendment 1: Application of risk management | |
| PARTITIONS, OFFICE, STEEL | |
| POINTER, LECTURE | |
| Preparation and quality management of fluids for haemodialysis and related therapies\x97 Part 4: Concentrates for haemodialysis and related therapies | |
| Preparation and quality management of fluids for haemodialysis and related therapies\x97Part 1: General requirements | |
| Preparation and quality management of fluids for haemodialysis and related therapies\x97Part 2: Water treatment equipment for haemodialysis applications and related therapies | |
| Preparation and quality management of fluids for haemodialysis and related therapies\x97Part 3: Water for haemodialysis and related therapies | |
| Preparation and quality management of fluids for haemodialysis and related therapies\x97Part 5: Quality of dialysis fluid for haemodialysis and related therapies | |
| PRESSURE REFUELLING CONNECTIONS AND DEFUELLING FOR AIRCRAFT | |
| Processing of health care products\x97Informat ion to be provided by the medical device manufacturer for the processing of medical devices\x97Part 1: Critical and semi-critical medical devices | |
| Processing of health care products\x97Informat ion to be provided by the medical device manufacturer for the processing of medical devices\x97Part 2: Non-critical medical devices | |
| PRODUCTION, MAINTENANCE AND MANAGEMENT OF NATO STANDARDIZATION DOCUMENTS | |
| PUBLISHING STANDARDS FOR ALLIED PUBLICATIONS | |
| PUBLISHING STANDARDS FOR NATO STANDARDIZATION DOCUMENTS | |
| RACK, CLOTHING, SEMI-CONCEALED | |
| RACK, DISPLAY, BOOK, (WOOD) | |
| RACK, STORAGE, DATA TAPE | |
| RACKS, STORAGE, GENERAL PURPOSE | |
| RACKS, WEARING APPAREL, STEEL | |
| RECOMMENDED AIR-TO-AIR REFUELLING (AAR) AIRCREW CERTIFICATION AND CURRENCY | |
| REFRIGERATOR, MECHANICAL, COMMERCIAL, SELF-CONTAINED, REACH-IN AND PASS-THROUGH | |
| REFRIGERATORS, MECHANICAL, HOUSEHOLD (ELECTRICAL, SELF-CONTAINED) | |
| SAFE, DENTAL X-RAY FILM PROTECTIVE | |
| SAFE, OFFICE, FIRE RESISTANT, BURGLARY PROTECTION | |
| SAFE, TOOL-RESISTANT, UNINSULATED, SECURITY | |
| SAFETY AND SUITABILITY FOR SERVICE ASSESSMENT TESTING FOR MEDIUM CALIBRE AMMUNITION FROM 20 mm TO 40 mm | |
| SAFETY AND SUITABILITY FOR SERVICE ASSESSMENT TESTING FOR MORTAR CARTRIDGES | |
| SAFETY AND SUITABILITY FOR SERVICE ASSESSMENT TESTING OF NON-NUCLEAR MUNITIONS | |
| SCREEN, BEDSIDE (ALUMINUM) | |
| Selection and Applications | |
| SHELF, FILING | |
| SHELVING, STORAGE AND DISPLAY, STEEL, BOLTLESS | |
| SHELVING, STORAGE AND DISPLAY, STEEL, CLIP TYPE | |
| SHELVING, STORAGE AND DISPLAY, STEEL, INTERCHANGEABLE, NUT AND BOLT TYPE | |
| Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements | |
| Small-bore connectors for liquids and gases in healthcare applications - Part 20: Common test methods | |
| Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 | |
| Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications | |
| Small-bore connectors for liquids and gases in healthcare applications - Part 6: Connectors for neuraxial applications | |
| Small-bore connectors for liquids and gases in healthcare applications-Part 5: Connectors for limb cuff inflation applications | |
| Small-bore connectors for liquids and gases in healthcare applications-Part 7: Connectors for intravascular or hypodermic applications | |
| Standard for Interoperable Item Development Life Cycle | |
| Standard for Interoperable Item Integration Life Cycle | |
| Standard for Risk Concerns for Interoperable Medical Products | |
| STANDS, DICTIONARY, WOOD | |
| STANDS, OFFICE MACHINE | |
| STANDS, SMOKING | |
| STANDS, TELEPHONE, STEEL, CONTEMPORARY STYLE | |
| STANDS, TYPEWRITER, WOOD | |
| Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices | |
| Sterilization of health care products - Ethylene oxide - Requirements for development, validation and routine control of a sterilization process for medical devices | |
| Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices | |
| Sterilization of health care products - Moist Heat - Guidance on the designation of a medical product to a product family and processing category for steam sterilization | |
| Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | |
| Sterilization of health care products \x96 Moist Heat \x96 Part 2: Guidance on the application of ANSI/AAMI/ISO 17665-1 | |
| Sterilization of health care products \x97 Chemical indicators \x97 Guidance for selection, use and interpretation of results | |
| Sterilization of health care products \x97 Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives \x97 Requirements for characterization, development, validation and routine control of... | |
| Sterilization of health care products-Microbiolog ical methods-Part 1: Determination of a population of microorganisms on products | |
| Sterilization of health care products-Moist heat-Part 1: Requirements for the development, validation, and routine control of a sterilization process for medical devices | |
| Sterilization of health care products\x97 Chemical indicators\x97Part 4: Class 2 indicators as an alternative to the Bowie and Dick-type test for detection of steam penetration | |
| Sterilization of health care products\x97 Chemical indicators\x97Part 5: Class 2 indicators for Bowie and Dick-type air removal tests | |
| Sterilization of health care products\x97 Microbiological methods\x97Part 1: Determination of a population of microorganisms on products AMENDMENT 1 | |
| Sterilization of health care products\x97 Radiation\x97Part 1: Requirements for development, validation, and routine control of a sterilization process for medical devices | |
| Sterilization of health care products\x97Biologic al and chemical indicators\x97Test equipment | |
| Sterilization of health care products\x97Biologic al indicators\x97Part 1: General requirements | |
| Sterilization of health care products\x97Biologic al indicators\x97Part 2: Biological indicators for ethylene oxide sterilization processes | |
| Sterilization of health care products\x97Biologic al indicators\x97Part 3: Biological indicators for moist heat sterilization processes | |
| Sterilization of health care products\x97Biologic al indicators\x97Part 4: Biological indicators for dry heat sterilization processes | |
| Sterilization of health care products\x97Biologic al indicators\x97Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes | |
| Sterilization of health care products\x97Biologic al indicators\x97Part 7: Guidance for the selection, use and interpretation of results | |
| Sterilization of health care products\x97Biologic al indicators\x97Part 8: Method for validation of a reduced incubation item for a biological indicator | |
| Sterilization of health care products\x97Chemical indicators\x97Part 1: General requirements | |
| Sterilization of health care products\x97Chemical indicators\x97Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test | |
| Sterilization of health care products\x97Chemical indicators\x97Part 6: Type 2 indicators and process challenge devices for use in performance testing of small steam sterilizers | |
| Sterilization of health care products\x97Guidance on the requirements for the validation and routine processing of ethylene oxide sterilization processes using parametric release | |
| Sterilization of health care products\x97Microbio logical methods\x97Guidance on conducting bioburden determinations and tests of sterility for biologics and tissue-based products | |
| Sterilization of health care products\x97Radiatio n\x97Part 3: Guidance on dosimetric aspects of development, validation and routine control | |
| Sterilization of health care products\x97Radiatio n\x97Part 4: Guidance on process control | |
| Sterilization of health care products\x97Radiatio n\x97Substantiation of selected sterilization dose: Method VDmax SD | |
| Sterilization of health-care products\x97Ethylene oxide\x97Requirement s for the development, validation and routine control of a sterilization process for medical devices\x97 Amendment 1: Revision of Annex E, Single batch release | |
| Sterilization of medical devices\x97Microbiol ogical methods\x97Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process | |
| STOOL, REVOLVING, SURGEON'S | |
| STOOL, STEP, CASTER MOUNTED, SAFETY | |
| STOOL, STRAIGHT | |
| STOOLS, FILING AND GENERAL PURPOSE, STEEL | |
| STOOLS, REVOLVING | |
| STOOLS, STEP, STEEL, FOLDING STEPS | |
| STORAGE SECTION, OVER-FILE | |
| STORAGE SECTION, STEEL X-RAY | |
| STORAGE SECTIONS, OVERFILE, STEEL, CONTEMPORARY STYLE | |
| SYMBOL MARKING OF AIRCRAFT SERVICING AND SAFETY/HAZARDS POINTS | |
| TABLE, ANESTHETIST'S | |
| TABLE, BEDSIDE, METAL | |
| TABLE, EXAMINING | |
| TABLE, FOLDING, STEEL TUBE (ADVANCE BASE) | |
| TABLE, OFFICE (STEEL, CONTEMPORARY STYLE) | |
| TABLE, WOOD GENERAL OFFICE | |
| TABLE, WRITING, DOUBLE WITH STATIONARY RACK | |
| TABLES, STEEL, GENERAL OFFICE | |
| TABLES, SURGICAL INSTRUMENT AND SURGICAL DRESSING (MOBILE) | |
| TABLES, WOOD OR METAL, BASE | |
| TABLES: PARSONS, CUBE, DRUM AND PANEL | |
| TANKER CAPABILITIES | |
| TANKER/RECEIVER CLEARANCE - TECHNICAL COMPATIBILITY MATRIX | |
| THE PROVISION OF HYDRAULIC POWER FOR SERVICING AIRCRAFT HYDRAULIC SYSTEMS | |
| TOP AND SHELF ASSEMBLY, STEEL, UNITIZED | |
| TRAY, DESK, STEEL, AND SUPPORT SET, STACKING | |
| TRAY, DESK, WOOD, EXECUTIVE OFFICE TYPE | |
| TRAY, DESK; AND SUPPORT SET, STACKING DESK TRAY | |
| TRAY, STATIONARY, METAL, FOR STEEL DESKS | |
| TRAYS, ASH | |
| TYRE VALVE COUPLINGS |
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