医疗类标准(二)
2019-07-23 21:39标准号 | 中文名称 | 英文名称 |
KS P ISO 11953-2012 | 牙科-植入物-手扭距仪的临床性能 | Dentistry-Implants-Clinical performance of hand torque instruments |
KS P ISO 11140-1-2012 | 眼科植入物.眼内透镜.第1部分:词汇 | Ophthalmic implants — Intraocular lenses — Part 1: Vocabulary |
KS P ISO 11140-2-2002 | 眼科植入物.眼内透镜.第3部分:机械性能和试验方法 | Ophthalmic implants — Intraocular lenses — Part 3: Mechanical properties and test methods |
KS P ISO 11140-3-2009 | 眼科植入物.眼内透镜.第4部分:标签和信息 | Ophthalmic implants — Intraocular lenses — Part 4: Labelling and information |
KS P ISO 11140-4-2009 | 眼科植入物人工晶状体第5部分:生物相容性 | Ophthalmic implants-Intraocular lenses-Part 5:Biocompatibility |
KS P ISO 11140-5-2009 | 眼科植入物人工晶状体第6部分:保存期和运输稳定性 | Ophthalmic implants-Intraocular lenses-Part 6:Shelf-life and transport stability |
KS P ISO 11199-1-2014 | 眼科植入物人工晶状体第7部分:临床研究 | Ophthalmic implants-Intraocular lenses-Part 7:Clinical investigations |
KS P ISO 11199-2-2014 | 眼科植入物.眼内透镜.第8部分:基本要求 | Ophthalmic implants — Intraocular lenses — Part 8: Fundamental requirements |
KS P ISO 11980-2006 | 眼科光学.接触镜和接触镜保护产品.临床检测指南 | Ophthalmic optics-Contact lenses and contact lens care products-Guidance for clinical investigations |
KS P ISO 12189-2009 | 外科植入物可植入脊柱装置的机械试验使用前支架的脊柱植入装置疲劳试验方法 | Implants for surgery-Mechanical testing of implantable spinal devices-Fatigue test method for spinal implant assemblies using an anterior support |
KS P ISO 11199-3-2014 | 造口辅助设备用皮肤屏障.试验方法.第1部分:尺寸、表面pH值和吸水性 | Skin barrier for ostomy aids — Test methods — Part 1: Size, surface pH and water-absorbency |
KS P ISO 12865-2002 | 眼科仪器.检眼镜 | Ophthalmic instruments-Retinoscopes |
KS P ISO 12866-2002 | 眼科仪器.视野计 | Ophthalmic instruments-Perimeters |
KS P ISO 11334-1-2010 | 外科植入物的修复和分析.第1部分:修复和处理 | Retrieval and analysis of surgical implants — Part 1: Retrieval and handling |
KS P ISO 11334-4-2007 | 外科植入物的回收和分析第2部分:回收的金属外科植入物的分析 | Retrieval and analysis of surgical implants-Part 2:Analysis of retrieved metallic surgical implants |
KS P ISO 11418-1-2009 | 外科植入物的回收和分析第3部分:回收的聚合外科植入物的分析 | Retrieval and analysis of surgical implants-Part 3:Analysis of retrieved polymeric surgical implants |
KS P ISO 11418-2-2009 | 外科植入物的回收和分析第4部分:回收的陶瓷外科植入物的分析 | Retrieval and analysis of surgical implants-Part 4:Analysis of retrieved ceramic surgical implants |
KS P ISO 13017-2018 | 牙科学.磁性附件 | Dentistry — Magnetic attachments |
KS P ISO 13116-2017 | 牙科材料放射性不透明度测定方法 | Dentistry ─ Test Method for Determining Radio-Opacity of Materials |
KS P ISO 13295-2008 | 牙科旋转器械心轴 | Dentistry-Mandrels for rotary instruments |
KS P ISO 13356-2009 | 外科植入物基于钇稳定四方氧化锆(Y-TZP)的陶瓷材料 | Implants for surgery-Ceramic materials based on yttria-stabilized tetragonal zirconia(Y-TZP) |
KS P ISO 11418-3-2009 | 牙周刮匙、牙科刮除器和牙钻孔器.第1部分:一般要求 | Periodontal curettes, dental scalers and excavators — Part 1:General requirements |
KS P ISO 11418-4-2009 | 牙科学.牙周刮匙、牙刮除器和牙钻孔器.第2部分:Gr型牙周刮匙 | Dentistry — Periodontal curettes, dental scalers and excavators — Part 2: Periodontal curettes of Gr-type |
KS P ISO 11418-5-2009 | 牙周刮匙、牙刮除器和牙钻孔器.第4部分:牙钻孔器.盘状 | Periodontal curettes, dental scalers and excavators — Part 4: Dental excavators — Discoid type |
KS P ISO 13402-2008 | 外科和牙科手用器械耐高压灭菌、耐腐蚀和耐热性的测定 | Surgical and dental hand instruments-Determination of resistance against autoclaving, corrosion and thermal exposure |
KS P ISO 13404-2012 | 假肢和矫形学外部矫形和矫形部件的分类和描述 | Prosthetics and orthotics-Categorization and description of external orthoses and orthotic components |
KS P ISO 11418-7-2009 | 修复和矫形学修复部件的分类和描述第1部分:修复部件的分类 | Prosthetics and orthotics-Classification and description of prosthetic components-Part 1:Classification of prosthetic components |
KS P ISO 11607-1-2007 | 假肢和矫形学假肢部件的分类和描述第2部分:下肢假肢部件的描述 | Prosthetics and orthotics-Classification and description of prosthetic components-Part 2:Description of lower-limb prosthetic components |
KS P ISO 11607-2-2007 | 假肢和矫形学假肢部件的分类和描述第3部分:上肢假肢部件的描述 | Prosthetics and orthostics-Classification and description of prosthetic components-Part 3:Description of upper-limb prosthetic components |
KS P ISO 11737-1-2012 | 保健产品无菌加工第1部分:一般要求 | Aseptic processing of health care products-Part 1:General requirements |
KS P ISO 11737-2-2012 | 保健产品无菌加工第2部分:过滤 | Aseptic processing of health care products-Part 2:Filtration |
KS P ISO 11979-1-2017 | 保健品无菌加工第3部分:冻干 | Aseptic processing of health care products-Parts 3:Lyophilization |
KS P ISO 11979-3-2017 | 保健产品无菌加工第4部分:就地清洁技术 | Aseptic processing of health care products-Part 4:Clean-in-place technologies |
KS P ISO 11979-4-2017 | 保健品无菌加工第5部分:就地灭菌 | Aseptic processing of healthcare products-Part 5:Sterilization in place |
KS P ISO 11979-5-2006 | 保健产品无菌加工第6部分:隔离系统 | Aseptic processing of health care products-Part 6:Isolator systems |
KS P ISO 13485-2007 | 医疗器械质量管理体系监管要求 | Medical devices-Quality management systems-Requirements for regulatory purposes |
KS P ISO 11979-6-2006 | 轮椅.第1部分:ISO 7176系列轮椅应用指南 | Wheelchairs-Part 1:Guidelines for the application of the ISO 7176 series on wheelchairs |
KS P ISO 13716-2014 | 可逆和不可逆水解胶体印模材料系统 | Dentistry — Reversible-irreversible hydrocolloid impression material systems |
KS P ISO 11979-7-2006 | 乳酸羟基磷灰石植入物:脑羟基磷灰石 | Implants for surgery — Hydroxyapatite — Part 1: Ceramic hydroxyapatite |
KS P ISO 11979-8-2017 | 增殖羟基磷灰石植入物:羟基磷灰石涂层 | Implants for surgery — Hydroxyapatite — Part 2: Coatings of hydroxyapatite |
KS P ISO 12505-1-2016 | 促肾上腺皮质植入物的植入物第三部分:晶体化学分析与表征 | Implants for surgery-Hydroxyapatite-Part 3:Chemical analysis and characterization of crystallinity and phase purity |
KS P ISO 12891-1-2014 | 促肾上腺皮质植入物第4部分:凝固粘附强度的测定 | Implants for surgery-Hydroxyapatite-Part 4:Determination of coating adhesion strength |
KS P ISO 13781-2008 | 外科植入物.用聚L-交酯树脂及制品体外降解试验 | Poly(L-lactide) resins and fabricated forms for surgical implants-In vitro degradation testing |
KS P ISO 13782-2009 | 外科植入物.金属材料.外科植入用纯钽材料 | Implants for surgery-Metallic materials-Unalloyed tantalum for surgical implant applications |
KS P ISO 13897-2018 | 牙科学.汞齐合金胶囊 | Dentistry-Amalgam capsules |
KS P ISO 12891-2-2008 | 注射笔系统.第1部分:医用针头注射器用玻璃套筒 | Pen systems-Part 1:Glass cylinders for pen-injectors for medical use |
KS P ISO 12891-3-2008 | 注射笔系统.第2部分:医用笔式注射器的柱塞和盘 | Pen systems-Part 2:Plungers and discs for pen-injectors for medical use |
KS P ISO 13958-2009 | 血液透析和相关治疗的浓缩物 | Concentrates for haemodialysis and related therapies |
KS P ISO 13959-2009 | 血液透析用水和有关疗法 | Water for haemodialysis and related therapies |
KS P ISO 13960-2017 | 心血管植入物与人造器官.血浆过滤器 | Cardiovascular implants and extracorporeal systems — Plasmafilters |
KS P ISO 12891-4-2008 | 人体医疗器械临床调查第1部分:一般要求 | Clinical investigation of medical devices for human subjects-Part 1:General requirements |
KS P ISO 13397-1-2018 | 人体医疗器械临床调查第2部分:临床调查方案 | Clinical investigation of medical devices for human subjects-Part 2:Clinical investigation plans |
KS P ISO 14161-2012 | 医疗保健产品灭菌生物指标选择、使用和结果解释指南 | Sterilization of health care products-Biological indicators-Guidance for the selection, use and interpretation of results |
KS P ISO 14233-2004 | 牙科学.聚合基模具材料 | Dentistry-Polymer-based die materials |
KS P ISO 13397-2-2018 | 外科植入物全髋关节假体的磨损第1部分:磨损试验机的载荷和位移参数及试验的相应环境条件 | Implants for surgery-Wear of total hip-joint prostheses- Part 1:Loading and displacement parameters for wear-testing machines and corresponding environmental conditions for test |
KS P ISO 13397-4-2018 | 外科植入物全髋关节假体的磨损第2部分:测量方法 | Implants for surgery-Wear of total hip-joint prostheses-Part 2:Methods of measurement |
KS P ISO 13405-1-2016 | 外科植入物.全膝关节假体的磨损.第1部分:磨损试验机的负荷控制和相应的试验环境条件的负荷和位移参数 | Implants for surgery-Wear of total knee-joint prostheses- Part 1:Loading and displacement parameters for wear-testing machines with load control and corresponding environmental conditions for test |
KS P ISO 13405-2-2016 | 外科植入物.全膝关节假肢的磨损.第2部分:测量方法 | Implants for surgery — Wear of total knee-joint prostheses — Part 2: Methods of measurement |
KS P ISO 13405-3-2016 | 外科植入物.全膝关节假体的磨损.第3部分:带位移控制的磨损试验机的负荷和位移参数及试验的相应环境条件 | Implants for surgery-Wear of total knee-joint prostheses-Part 3:Loading and displacement parameters for wear-testing machines with displacement control and corresponding environmental conditions for test |
KS P ISO 14356-2014 | 牙科学.复制材料 | Dentistry — Duplicating material |
KS P ISO 14408-2009 | 激光手术用气管掐管.标识及附带信息要求 | Tracheal tubes designed for laser surgery-Requirements for marking and accompanying information |
KS P ISO 14457-2017 | 牙科-机头和电机 | Dentistry ─ Handpieces and motors |
KS P ISO 14602-2017 | 固定外科植入物.骨接合术用植入物.特殊要求 | Non-active surgical implants-Implants for osteosynthesis-Particular requirements |
KS P ISO 14607-2009 | 外科植入物.乳房植入物的特殊要求 | Implants for surgery-Specific requirements for mammary implants |
KS P ISO 14630-2009 | 非活动外科植入物的一般要求 | Non-active surgical implants-General requirements |
KS P ISO 13408-1-2017 | 外科植入物有源可植入医疗器械第1部分:安全、标记和制造商提供信息的一般要求 | Implants for surgery-Active implantable medical devices-Part 1:General requirements for safety, marking and for information to be provided by the manufacturer |
KS P ISO 13408-2-2010 | 外科植入物有源可植入医疗器械第2部分:心脏起搏器 | Implants for surgery-Active implantable medical devices-Part 2:Cardiac pacemakers |
KS P ISO 13408-3-2010 | 外科植入物主动植入式医疗器械第3部分:植入式神经刺激器 | Implants for surgery-Active implantable medical devices-Part 3:Implantable neurostimulators |
KS P ISO 13408-4-2010 | 外科植入物有源可植入医疗器械第4部分:可植入输液泵 | Implants for surgery-Active implantable medical devices-Part 4:Implantable infusion pumps |
KS P ISO 13408-5-2010 | 外科植入物有源可植入医疗器械第5部分:循环支持设备 | Implants for surgery-Active implantable medical devices-Part 5:Circulatory support devices |
KS P ISO 14801-2013 | 牙科植入物骨内植入物动态疲劳试验方法 | Dentistry-Implants-Dynamic fatigue test for endosseous dental implants |
KS P ISO 13408-6-2017 | 外科植入物.全膝关节假体.第1部分:胫骨部件疲劳性能的测定 | Implants for surgery-Total knee-joint prostheses-Part 1:Determination of endurance properties of knee tibial trays |
KS P ISO 14937-2012 | 医疗保健产品灭菌灭菌剂特性及医疗器械灭菌过程的开发、验证和常规控制的一般要求 | 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 |
KS P ISO 14949-2009 | 外科植入物.两部分辅助治疗聚硅酮弹性材料 | Implants for surgery-Two-part addition-cure silicone elastomers |
KS P ISO 15010-2018 | 输血和输液瓶用用弃式悬挂装置.要求和试验方法 | Disposable hanging devices for transfusion and infusion bottles — Requirements and test methods |
KS P ISO 15032-2005 | 修复术.髋关节结构试验 | Prostheses-Structural testing of hip units |
KS P ISO 13779-1-2014 | 牙科起子.第1部分:一般要求 | Dental elevators — Part 1: General requirements |
KS P ISO 13779-2-2014 | 牙科起子.第2部分:沃里克·詹姆斯起子 | Dental elevators — Part 2: Warwick James elevators |
KS P ISO 13779-3-2009 | 牙科起子.第3部分:Cryer起子 | Dental elevators — Part 3: Cryer elevators |
KS P ISO 13779-4-2009 | 牙科起子.第4部分:Coupland起子 | Dental elevators — Part 4: Coupland elevators |
KS P ISO 13926-1-2010 | 牙科起子.第5部分:BEIN起子 | Dental elevators — Part 5: Bein elevators |
KS P ISO 13926-2-2017 | 牙科起子.第6部分:Flohr起子 | Dental elevators — Part 6: Flohr elevators |
KS P ISO 14155-1-2007 | 牙科镊子.第1部分:一般要求 | Dental tweezers — Part 1: General requirements |
KS P ISO 14155-2-2007 | 牙科镊子.第2部分:Meriam型 | Dental tweezers — Part 2: Meriam types |
KS P ISO 14242-1-2009 | 牙科镊子第3部分:学院型 | Dental tweezers-Part 3:College types |
KS P ISO 14242-2-2007 | 外科植入物金属髓内钉系统第1部分:髓内钉 | Implants for surgery-Metal intramedullary nailing systems-Part 1:Intramedullary nails |
KS P ISO 14243-1-2009 | 外科植入物金属髓内钉系统第2部分:锁定部件 | Implants for surgery-Metal intramedullary nailing systems-Part 2:Locking components |
KS P ISO 14243-2-2014 | 外科植入物金属髓内钉系统第3部分:连接装置和扩孔器直径测量 | Implants for surgery-Metal intramedullary nailing systems-Part 3:Connection devices and reamer diameter measurements |
KS P ISO 15189-2013 | 医学实验室.质量和能力的特殊要求 | Medical laboratories ─ Requirements for quality and competence |
KS P ISO 15190-2010 | 医学实验室.安全要求 | Medical laboratories-Requirements for safety |
KS P ISO 15193-2014 | 实验室条件下医用诊断装置.生物原始试样中数量值的测量.参考测量法的说明 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement procedures |
KS P ISO 15194-2014 | 实验室条件下医用诊断装置.生物原始试样中数量值的测量.标准物质的描述 | In virto diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation |
KS P ISO 15195-2014 | 实验室医学.参考测量实验室的要求 | Laboratory medicine — Requirements for reference measurement laboratories |
KS P ISO 15197-2017 | 体外诊断试验系统.糖尿病症管理中自测用血糖监测系统的要求 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus |
KS P ISO 15198-2017 | 临床实验室药物.体外诊断医疗设备.由制造商证实的用户质量控制程序 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer |
KS P ISO 15223-2007 | 医疗器械.用于医疗器械标签、作标记和提供信息的符号 | Medical devices-Symbols to be used with medical device labels, labelling and information to be supplied |
KS P ISO 15225-2014 | 医疗器械.质量管理.医疗器械命名数据结构 | Medical devices — Quality management — Medical device nomenclature data structure |
KS P ISO 15374-2009 | 外科植入物.锻件生产要求 | Implants for surgery-Requirements for production of forgings |
KS P ISO 15606-2012 | 牙科手机.气动刮器和刮器梢尖 | Dental handpieces-Air-powered scalers and scaler tips |
KS P ISO 15621-2007 | 吸尿器材评定的一般指南 | Urine-absorbing aids-General guidance on evaluation |
KS P ISO 1563-2009 | 牙科用藻酸盐牙印模 | Dental alginate impression material |
KS P ISO 1564-2012 | 牙科琼脂基水胶仿印模材料 | Dental aqueous impression materials based on agar |
KS P ISO 15674-2009 | 心血管植入物和人工器官-硬壳式心脏切除术/静脉储备系统(有/无过滤器)和软静脉储备袋 | Cardiovascular implants and artificial organs-Hard-shell cardiotomy/venous reservoir systems(with/without filter) and soft venous reservoir bags |
KS P ISO 15675-2009 | 心血管植入物和人工器官-心肺转流系统-动脉血液过滤器 | Cardiovascular implants and artificial organs-Cardiopulmonary bypass systems-Arterial blood line filters |
KS P ISO 15676-2007 | 心血管植入物和人工器官体外循环(CBP)和体外膜氧合(ECMO)一次性导管包装要求 | Cardiovascular implants and artificial organs-Requirements for single-use tubing packs for cardiopulmonary bypass(CBP) and extracorporeal membrane oxygenation(ECMO) |
KS P ISO 15747-2008 | 静脉注射用塑料容器 | Plastics containers for intravenous injection |
KS P ISO 15752-2006 | 眼科仪器.内发光器.光辐射安全的基本要求和试验方法 | Ophthalmic instruments-Endoilluminators-Fundamentalrequirements and test methods for optical radiation safety |
KS P ISO 15798-2006 | 眼科植入物.眼科手术粘接器件 | Ophthalmic implants-Ophthalmic viscosurgical devices |
KS P ISO 15814-2008 | 外科植入物.聚合交脂基共聚物及混料.体外降解试验 | Implants for surgery-Copolymers and blends based on polylactide-In vitro degradation testing |
KS P ISO 15841-2017 | 牙科学.正畸用金属丝 | Dentistry — Wires for use in orthodontics |
KS P ISO 15854-2013 | 牙科铸造和基板蜡 | Dentistry-Casting and baseplate waxes |
KS P ISO 14243-3-2009 | 洗涤器消毒剂第1部分:一般要求、术语、定义和试验 | Washer-disinfectors-Part 1:General requirements,terms and definitions and tests |
KS P ISO 14708-1-2007 | 洗涤器消毒剂-第2部分:外科器械、麻醉设备、碗、碟、杯、器皿、玻璃器皿等采用热消毒的洗涤器消毒剂的要求和试验。 | Washer-disinfectors-Part 2:Requirements and tests for washer-disinfectors employing thermal disinfection for surgical instruments, anaesthetic equipment, bowls, dishes, receivers,utensils, glassware, etc. |
KS P ISO 14708-2-2014 | 洗涤消毒剂第3部分:用热消毒的洗涤消毒剂的要求和试验 | Washer-disinfectors-Part 3:Requirements and tests for washer-disinfectors employing thermal disinfection for |
KS P ISO 14708-3-2010 | 洗涤器消毒剂第4部分:不耐热内窥镜用化学消毒洗涤器消毒剂的要求和试验 | Washer-disinfectors-Part 4:Requirements and tests for washer-disinfectors employing chemical disinfection for thermolabile endoscopes |
KS P ISO 15912-2009 | 牙科铸造包埋材料和难熔模材料 | Dentistry-Casting investments and refractory die materials |
KS P ISO 16021-2011 | 吸尿辅助器具一次性使用成人失禁吸尿辅助器具使用者和护理者评价的基本原则 | Urine-absorbing aids-Basic principles for evaluation of single-use adult-incontinence-absorbing aids from the perspective of users and caregivers |
KS P ISO 16054-2009 | 外科植入物.外科植入物的最小数据集 | Implants for surgery-Minimum data sets for surgical implants |
KS P ISO 16059-2009 | 牙科学数据交换用编码所需的要素 | Dentistry-Required elements for codification used in data exchange |
KS P ISO 16061-2014 | 与非有源外科植入物相关的仪器.一般要求 | Instrumentation for use in association with non-active surgical implants — General requirements |
KS P ISO 16256-2017 | 临床实验室试验和体外诊断试验系统感染性疾病酵母菌抗菌剂体外活性检测的参考方法 | Clinical laboratory testing and in vitro diagnostic test systems ─ Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases |
KS P ISO 16391-2011 | 造口和尿失禁辅助器具灌洗器具要求和试验方法 | Aids for ostomy and incontinence-Irrigation sets-Requirements and test methods |
KS P ISO 16402-2009 | 外科植入物-丙烯酸树脂水泥-骨科用丙烯酸树脂水泥的弯曲疲劳试验 | Implants for surgery-Acrylic resin cement-Flexural fatigue testing of acrylic resin cements used in orthopaedics |
KS P ISO 16408-2014 | 牙科学.口腔卫生产品.口腔冲洗 | Dentistry — Oral hygiene products — Oral rinses |
KS P ISO 16409-2017 | 牙科-口腔卫生用品-手动齿间刷 | Dentistry-Oral hygiene products-Manual interdental brushes |
KS P ISO 16428-2007 | 外科植入物可植入材料和医疗器械静态和动态腐蚀试验的试验溶液和环境条件 | Implants for surgery-Test solutions and environmental conditions for static and dynamic corrosion tests on implantable materials and medical devices |
KS P ISO 16429-2010 | 外科植入物.金属可植入材料和过期医疗设备的开放电路潜在腐蚀性能测量 | Implants for surgery-Measurements of open-circuit potential to assess corrosion behaviour of etallic implantable materials and medical devices over extended time periods |
KS P ISO 16443-2017 | 牙科植入系统及相关程序词汇 | Dentistry ─ Vocabulary for dental implants systems and related procedure |
KS P ISO 14708-4-2010 | 牙科学.牙科橡胶坝器械.第2部分:钳子 | Dentistry ─ Dental rubber dam instruments ─ Part 2: Clamp forceps |
KS P ISO 16671-2006 | 眼科植入物.眼外科用冲洗法 | Ophthalmic implants-Irrigating solutions for ophthalmic surgery |
KS P ISO 16672-2006 | 外科植入物.眼内填塞 | Ophthalmic implants-Ocular endotamponades |
KS P ISO 14708-5-2012 | 轮椅座椅第1部分:词汇、基准轴惯例和人体节段、姿势和姿势支撑面的测量方法 | Wheelchair seating-Part 1:Vocabulary, reference axis convention and measures for body segments, posture and postural support surfaces |
KS P ISO 16840-10-2017 | 轮椅非整体式座椅和靠背支撑垫的耐燃性第10部分:要求和试验方法 | Wheelchairs ─ Resistance to ignition of non-integrated seat and back support cushions ─ Part 10: Requirements and test methods |
KS P ISO 14879-1-2008 | 轮椅座椅第2部分:管理组织完整性的装置的物理和机械特性的测定坐垫 | Wheelchair seating-Part 2:Determination of physical and mechanical characteristics of devices intended to manage tissue integrity-Seat cushions |
KS P ISO 14971-1-2002 | 轮椅座椅.第3部分:姿势支撑装置的静态、冲击和重复荷载强度的测定 | Wheelchair seating — Part 3: Determination of static, impact and repetitive load strengths for postural support devices |
KS P ISO 15087-1-2018 | 轮椅座椅第4部分:机动车辆用座椅系统 | Wheelchair seating-Part 4:Seating systems for use in motor vehicles |
KS P ISO 15087-2-2018 | 轮椅座椅第6部分:座垫性能变化的模拟使用和测定 | Wheelchair seating ─ Part 6: Simulated use and determination of the changes in properties of seat cushions |
KS P ISO 16954-2017 | 牙科学牙科单位水线生物膜处理试验方法 | Dentistry ─ Test methods for dental unit waterline biofilm treatment |
KS P ISO 15087-3-2018 | 尿失禁者用吸尿器材聚合物吸收材料特性的试验方法 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials- |
KS P ISO 17190-10-2011 | 尿失禁者用吸尿器材聚合物吸收材料特性的试验方法第10部分:电位滴定法测定可提取聚合物含量 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 10:Determination of extractable polymer content by potentiometric titration |
KS P ISO 17190-11-2011 | 尿失禁者用吸尿器材聚合物吸收材料特性的试验方法第11部分:可吸入颗粒物含量的测定 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 11:Determination of content of respirable particles |
KS P ISO 15087-4-2018 | 尿失禁者用吸尿器材聚合物吸收材料特性的试验方法第2部分:残留单体的测定 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 2:Determination of amount of residual monomers |
KS P ISO 15087-5-2018 | 尿失禁者用吸尿器材聚合物基吸水材料特性的试验方法第3部分:用筛析法测定粒径分布 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 3:Determination of particle size distribution by sieve fractionation |
KS P ISO 15087-6-2018 | 尿失禁者用吸尿器材聚合物吸收材料特性的试验方法第4部分:加热失重法测定含水量 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 4:Determination of moisture content by mass loss upon heating |
KS P ISO 15098-1-2018 | 尿失禁者用吸尿器材聚合物吸收材料特性的试验方法第5部分:盐溶液中自由膨胀容量的重量法测定 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 5:Gravimetric determination of free swell capacity in saline solution |
KS P ISO 15098-2-2018 | 尿失禁者用吸尿器材聚合物基吸水材料特性的试验方法第6部分:离心后盐水溶液中液体滞留量的重量法测定 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 6:Gravimetric determination of fluid retention capacity in saline solution after centrifugation |
KS P ISO 15098-3-2008 | 尿失禁者用吸尿器材聚合物吸收材料特性的试验方法第7部分:压力下吸收的重量法测定 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 7:Gravimetric determination of absorption under pressure |
KS P ISO 15142-1-2010 | 尿失禁者用吸尿器材聚合物吸收材料特性的试验方法第8部分:流量的重量法测定 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 8:Gravimetric determination of flowrate |
KS P ISO 15142-2-2010 | 尿失禁者用吸尿器材聚合物吸水材料特性的试验方法第9部分:密度的重量法测定 | Urine-absorbing aids for incontinence-Test methods for characterizing polymer-based absorbent materials-Part 9:Gravimetric determination of density |
KS P ISO 17191-2011 | 尿失禁者用吸尿器材空气中可呼吸聚丙烯酸酯高吸水材料的测定钠原子吸收光谱法测定收集盒中灰尘 | Urine-absorbing aids for incontinence-Measurement of airborne respirable polyacrylate superabsorbent materials-Determination of dust in collection cassettes by sodium atomic absorption spectrometry |
KS P ISO 17218-2016 | 一次性使用无菌丝状针 | Sterile filiform acupuncture needles for single use |
KS P ISO 17304-2017 | 牙科学聚合收缩:聚合物基修复材料聚合收缩的测定方法 | Dentistry ─ Polymerization shrinkage: Method for determination of polymerization shrinkage of polymer-based restorative materials |
KS P ISO 15142-3-2010 | 睡眠窒息呼吸治疗.第2部分:面罩和应用附件 | Sleep apnoea breathing therapy-Part 1:Sleep apnoea breathing therapy equipment |
KS P ISO 15883-1-2012 | 睡眠窒息呼吸治疗.第2部分:面罩和应用附件 | Sleep apnoea breathing therapy-Part 2:Masks and application accessories |
KS P ISO 17511-2010 | 体外诊断医疗装置.生物试样的定量测量.校准仪和控制材料赋值的计量溯源性 | In vitro diagnostic medical devices-Measurement of quantities in biological samples-Metrological traceability of values assigned to calibrators and control materials |
KS P ISO 17593-2009 | 临床实验室试验和体外医疗器械口服抗凝治疗自检测体外监测系统要求 | Clinical laboratory testing and in vitro medical devices-Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy |
KS P ISO 15883-2-2012 | 医疗保健产品灭菌湿热第1部分:医疗器械灭菌过程的制定、验证和常规控制要求 | Sterilization of health care products-Moist heat-Part 1:Requirements for the development, validation and routine control of a sterilization process for medical devices |
KS P ISO 17730-2017 | 牙科氟化物清漆 | Dentistry ─ Fluoride varnishes |
KS P ISO 17853-2009 | 植入材料的磨损.聚酯和金属磨损粒子.离析、表征和量化 | Wear of implant materials-Polymer and metal wear particles-Isolation, characterization and quantification |
KS P ISO 17937-2018 | 牙科-骨凿 | Dentistry ─ Osteotome |
KS P ISO 1797-1-2004 | 牙科旋转器械柄第1部分:金属柄 | Dental rotary instruments-Shanks-Part 1:Shanks made of metal |
KS P ISO 1797-2-2012 | 牙科旋转器械柄第2部分:塑料柄 | Dental rotary instrument-Shanks-Part 2:Shanks made of plastics |
KS P ISO 15883-3-2012 | 体外诊断医疗器械.制造商提供的信息(标签).第1部分:术语、定义和一般要求 | In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 1: Terms, definitions and general requirements |
KS P ISO 15883-4-2012 | 体外诊断医疗器械.制造商提供的信息(标签).第2部分:专业用体外诊断试剂 | In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 2: In vitro diagnostic reagents for professional use |
KS P ISO 16635-2-2017 | 体外诊断医疗器械.制造商提供的信息(标签).第3部分:专业用体外诊断仪器 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use |
KS P ISO 16840-1-2011 | 体外诊断医疗器械.制造商提供的信息(标签).第4部分:自我试验用体外诊断试剂 | In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 4: In vitro diagnostic reagents for self-testing |
KS P ISO 16840-2-2011 | 体外诊断医疗器械.制造商提供的信息(标签).第5部分:自我试验用体外诊断仪器 | In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 5: In vitro diagnostic instruments for self-testing |
KS P ISO 18153-2010 | 体外诊断医疗装置.生物样品的定量测量.校准仪和控制材料所赋酶的催化浓度值的计量溯源性 | 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 |
KS P ISO 16840-3-2017 | 外科植入物总椎间盘假体的磨损第1部分:磨损试验的载荷和位移参数及试验的相应环境条件 | Implants for surgery-Wear of total intervertebral spinal disc prostheses-Part 1:Loading and displacement parameters for wear testing and corresponding environmental conditions for test |
KS P ISO 19001-2017 | 实验室诊断医疗设备.生物着色用实验室诊断试剂生产厂商提供的信息 | In virto diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology |
KS P ISO 1942-2010 | 牙科学词汇 | Dentistry-Vocabulary |
KS P ISO 19610-2018 | 红参工业生产工艺通用要求 | General requirements for industrial manufacturing process of red ginseng |
KS P ISO 19611-2018 | 抽气拔罐装置 | Air extraction cupping device |
KS P ISO 20127-2009 | 牙科动力牙刷一般要求和试验方法 | Dentistry-Powered toothbrushes-General requirements and test methods |
KS P ISO 20160-2008 | 外科植入物金属材料α+β钛合金棒显微结构分类 | Implants for surgery-Metallic materials-Classification of microstructures for alpha+beta titanium alloy bars |
KS P ISO 16840-4-2011 | 临床实验室试验和体外诊断试验系统传染源药敏试验和抗菌药敏试验装置性能评价第1部分:抗菌剂体外抗感染性疾病中快速生长的需氧菌活性试验的参考方法 | Clinical laboratory testing and in vitro diagnostic test systems-Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices-Part 1:Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases |
KS P ISO 16840-6-2017 | 临床实验室试验和体外诊断试验系统传染源药敏试验和抗菌药敏试验装置性能评价第2部分:抗菌药敏试验装置性能评价 | Clinical laboratory testing and in vitro diagnostic test systems-Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices-Part 2:Evaluation of performance of antimicrobial susceptibility test devices |
KS P ISO 17190-1-2011 | 牙科学-基聚合物-第1部分:义齿基聚合物 | Dentistry-Base polymers-Part 1:Denture base polymers |
KS P ISO 17190-2-2011 | 牙科学-基础聚合物-第2部分:正畸基础聚合物 | Dentistry-Base polymers-Part 2:Orthodontic base polymers |
KS P ISO 21530-2018 | 牙科学.牙科设备表面用材料.耐化学消毒剂的测定 | Dentistry — Materials used for dental equipment surfaces — Determination of resistance to chemical disinfectants |
KS P ISO 21531-2014 | 牙科学牙科仪器用图形符号 | Dentistry-Graphical symbols for dental instruments |
KS P ISO 21533-2017 | 牙科.韧带内注射用可重复使用的管式注射器 | Dentistry-Reusable cartridge syringes intended for intraligamentary injections |
KS P ISO 21534-2009 | 非活性外科植入物.关节替代用植入物.特殊要求 | Non-active surgical implants-Joint replacement implants-Particular requirements |
KS P ISO 21535-2017 | 非活性外科植入物.关节替代用植入物.髋关节替代用植入物的特殊要求 | Non-active surgical implants — Joint replacement implants — Specific requirements for hip-joint replacement implants |
KS P ISO 21536-2009 | 非活性外科植入物.关节替代用植入物.膝关节替代用植入物的特殊要求 | Non-active surgical implants-Joint replacement implants-Specific requirements for knee-joint replacement implants |
KS P ISO 2157-2009 | 牙科旋转器械.公称直径和命名代码 | Dental rotary instruments-Nominal diameters and designation code number |
KS P ISO 21606-2009 | 牙科学-正畸用弹性辅助材料 | Dentistry-Elastomeric auxiliaries for use in orthodontics |
KS P ISO 21647-2010 | 医用电气设备呼吸气体监测仪基本安全和基本性能专用要求 | Medical electrical equipment-Particular requirements for the basic safety and essential performance of respiratory gas monitors |
KS P ISO 21671-2009 | 牙科旋转抛光机 | Dentistry-Rotary polishers |
KS P ISO 17190-3-2011 | 牙科学.牙周探头.第1部分:一般要求 | Dentistry — Periodontal probes — Part1: General requirements |
KS P ISO 17190-4-2011 | 牙科学.牙周探头.第2部分:名称与符号 | Dentistry — Periodontal probes — Part 2: Designation |
KS P ISO 22112-2009 | 牙科学人工牙修复术 | Dentistry-Artificial teeth for dental prostheses |
KS P ISO 22254-2014 | 牙科学.手动牙刷.簇状部分抗偏转性 | Dentistry — Manual toothbrushes — Resistance of tufted portion to deflection |
KS P ISO 22374-2014 | 牙科-牙科手机-电动刮除器和刮除器头 | Dentistry-Dental handpieces-Electrical-powered scalers and scaler tips |
KS P ISO 17190-5-2011 | 使用动物组织及其衍生物的医疗器械.第1部分:风险管理的应用 | Medical devices utilizing animal tissues and their derivatives — Part 1: Application of risk management |
KS P ISO 17190-6-2011 | 利用动物组织及其衍生物的医疗器械.第2部分:采购、收集和搬运的控制 | Medical devices utilizing animal tissues and their derivatives — Part 2: Controls on sourcing, collection and handling |
KS P ISO 17190-7-2011 | 利用动物组织及其衍生物的医疗器械第3部分:病毒和传染性海绵状脑病(TSE)药剂的消除和/或灭活的验证 | 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 |
KS P ISO 22523-2016 | 外部假肢修复和外部矫形器.要求和试验方法 | External limb prostheses and external orthoses — Requirements and test methods |
KS P ISO 22674-2009 | 牙科固定和可移动修复和器具用金属材料 | Dentistry-Metallic materials for fixed and removable restorations and appliances |
KS P ISO 22675-2016 | 修复术.踝足装置和足部装置的试验.要求和试验方法 | Prosthetics — Testing of ankle-foot devices and foot units — Requirements and test methods |
KS P ISO 22794-2009 | 牙科学-口腔颌面外科中用于骨填充和增强的可植入材料-技术文件的内容 | Dentistry-Implantable materials for bone filling and augmentation in oral and maxillofacial surgery-Contents of a technical file |
KS P ISO 22803-2013 | 牙科学口腔颌面外科引导组织再生用膜材料技术文件的内容 | Dentistry-Membrane materials for guided tissue regeneration in oral and maxillofacial surgery-Contents of a technical file |
KS P ISO 22870-2009 | 护理点测试(POCT)——质量和能力要求 | Point-of-care testing(POCT)-Requirements for quality and competence |
KS P ISO 23317-2009 | 外科植入物植入材料磷灰石形成能力的体外评价 | Implants for surgery-In vitro evaluation for apatite-forming ability of implant materials |
KS P ISO 17190-8-2011 | 麻醉和呼吸用呼吸系统过滤器.第2部分:非过滤特性 | Breathing system filters for anaesthetic and respiratory use-Part 2:Non-filtration aspects |
KS P ISO 23600-2011 | 视力障碍者和视力、听力障碍者辅助产品行人交通信号灯的声音和触觉信号 | Assistive products for persons with vision impairments and persons with vision and hearing impairments-Acoustic and tactile signals for pedestrian traffic lights |
KS P ISO 23640-2013 | 体外诊断医疗器械.体外诊断试剂稳定性评价 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents |
KS P ISO 24214-2016 | 造口辅助设备用皮肤屏障.词汇 | Skin barrier for ostomy aids — Vocabulary |
KS P ISO 24234-2014 | 牙科学.牙科汞齐合金用汞及合金 | Dentistry-Mercury and alloys for dental amalgam |
KS P ISO 17190-9-2011 | 步行辅助用品提示要求和试验方法第1部分:提示摩擦 | Tips for assistive products for walking-Requirements and test methods-Part 1:Friction of tips |
KS P ISO 17510-1-2009 | 步行辅助用品提示要求和试验方法第2部分:拐杖提示耐久性 | Tips for assistive products for walking-Requirements and test methods-Part 2:Durability of tips for crutches |
KS P ISO 17510-2-2009 | 心血管植入物.血管内装置.第1部分:血管内修复 | Cardiovascular implants — Endovascular devices — Part 1: Endovascular prostheses |
KS P ISO 17665-1-2008 | 心血管植入物血管内装置第2部分:血管支架 | Cardiovascular implants-Endovascular devices-Part 2:Vascular stents |
KS P ISO 27020-2018 | 牙科学.正畸学用支架和管 | Dentistry — Brakets and tubes for use in orthodontics |
KS P ISO 28158-2017 | 牙科学综合牙线和手柄 | Dentistry-Integrated dental floss and handles |
KS P ISO 28319-2017 | 牙科-激光焊接 | Dentistry-Laser welding |
KS P ISO 28399-2013 | 牙科学.外部牙齿漂白用产品 | Dentistry — Products for external tooth bleaching |
KS P ISO 18113-1-2018 | 修复术和矫形学.词汇.第2部分:修复步态 | Prosthetics and orthotics — Vocabulary — Part 2: Prosthetics gait |
KS P ISO 3107-2014 | 牙科学.氧化锌/丁香酚粘合剂和氧化锌/非丁香酚粘合剂 | Dentistry — Zinc oxide/eugenol cements and zinc oxide/non-eugenol cements |
KS P ISO 3630-1-2012 | 牙科学牙根管器械第1部分:一般要求和试验方法 | Dentistry-Root-canal instruments-Part 1:General requirements and test methods |
KS P ISO 3630-2-2004 | 牙根管器械第2部分:扩张器 | Dental root-canal instruments-Part 2:Enlargers |
KS P ISO 3630-3-2012 | 牙根管器械第3部分:冷凝器、充填器和扩张器 | Dental root-canal instruments-Part 3:Condensers, pluggers and spreaders |
KS P ISO 3630-4-2017 | 牙科牙根管器械第4部分:辅助器械 | Dentistry-Root canal instruments-Part 4:Auxiliary instruments |
KS P ISO 3630-5-2013 | 牙科学.牙髓器械.第5部分:成形和清洁器械 | Dentistry — Endodontic instruments — Part 5: shaping and cleaning instruments |
KS P ISO 3665-2008 | 摄影.牙科用射线照相胶片.规范 | Photography-Intra-oral dental radiographic film-Specification |
KS P ISO 3823-1-2013 | 牙科旋转器械牙钻第1部分:钢制牙钻和硬质合金牙钻 | Dental rotary instruments-Burs-Part 1:Steel and carbide burs |
KS P ISO 3823-2-2012 | 牙科旋转牙钻器械第2部分:精加工牙钻 | Dentistry-Rotary bur instruments-Part 2:Finishing burs |
KS P ISO 3950-2008 | 牙科学牙齿和口腔区域的命名系统 | Dentistry-Designation system for teeth and areas of the oral cavity |
KS P ISO 4049-2017 | 牙科学.聚合物基修复材料 | Dentistry — Polymer-based restorative materials |
KS P ISO 4073-2017 | 牙科设备.牙科治疗室设备项目.识别体系 | Dentistry-Information system on the location of dental equipment in the working area of the oral health care provider |
KS P ISO 4135-2014 | 麻醉和呼吸设备.词汇 | Anaesthetic and respiratory equipment — Vocabulary |
KS P ISO 4823-2013 | 牙科弹性印模材料 | Dentistry-Elastomeric impression materials |
KS P ISO 5356-1-2009 | 麻醉和呼吸设备圆锥形连接器第1部分:锥体和插孔 | Anaesthetic and respiratory equipment-Conical connectors-Part 1:Cones and sockets |
KS P ISO 5356-2-2009 | 麻醉和呼吸设备锥形连接器第2部分:螺纹承重连接器 | Anaesthetic and respiratory equipment-Conical connectors-Part 2:Screw-threaded weight-bearing connectors |
KS P ISO 5358-2010 | 人用麻醉机 | Anaesthetic machines for use with humans |
KS P ISO 5361-2017 | 麻醉和呼吸设备气管导管和连接器 | Anaesthetic and respiratory equipment-Tracheal tubes and connectors |
KS P ISO 5362-2012 | 麻醉剂储存袋 | Anaesthetic reservoir bags |
KS P ISO 5364-2009 | 麻醉和呼吸设备.口咽通气管 | Anaesthetic and respiratory equipment-Oropharyngeal airways |
KS P ISO 5366-1-2009 | 麻醉和呼吸设备气管造口术用导管第1部分:成人用导管和连接器 | Anaesthetic and respiratory equipment-Tracheostomy tubes-Part 1:Tubes and connectors for use in adults |
KS P ISO 5366-3-2009 | 麻醉呼吸设备气管造口管第3部分:小儿气管造口管 | Anaesthetic and respiratory equipment-Tracheostomy tubes-Part 3:Paediatric tracheostomy tubes |
KS P ISO 5367-2009 | 麻醉机和通气机连用的呼吸管 | Breathing tubes intended for use with anaesthetic apparatus and ventilators |
KS P ISO 5799-2008 | 摄影.医用和牙科用直接爆光射线摄影胶片/处理系统.ISO感光速度和ISO平均梯度的测定 | Photography-Direct-exposing medical and dental radiographic film/process systems-Determination of ISO speed and ISO average gradient |
KS P ISO 5832-1-2012 | 外科植入物金属材料第1部分:锻制不锈钢 | Implants for surgery-Metallic materials-Part 1:Wrought stainless steel |
KS P ISO 18113-3-2015 | 外科植入物金属材料第11部分:钛6铝7铌合金 | Implant for surgery-Metallic materials-Part 11:Wrought titanium 6-aluminium 7-niobium alloy |
KS P ISO 18113-4-2015 | 外科植入物金属材料第12部分:可锻钴铬钼合金 | Implants for surgery-Mrtallic materials-Part 12:Wrought cobalt-chromium-molybdenum alloy |
KS P ISO 18113-5-2015 | 外科植入物金属材料第14部分:钛15钼5锆3铝合金 | Implants for surgery-Metallic materials-Part 14:Wrought titanium 15-molybdenum 5-zirconium 3-aluminium alloy |
KS P ISO 5832-2-2007 | 外科植入物金属材料第2部分:非合金钛 | Implants for surgery-Metallic materials-Part 2:Unalloyed titanium |
KS P ISO 5832-3-2007 | 外科材料金属材料第3部分:钛6-铝4-钒变形合金 | Imlants for surgery-Metallic materials-Part 3:Wrought titanium 6-aluminium 4-vanadium alloy |
KS P ISO 5832-4-2007 | 外科植入物金属材料第4部分:钴铬钼铸造合金 | Implants for surgery-Metallic materials-Part 4:Cobalt-chromium-molybdeum casting alloy |
KS P ISO 5832-5-2007 | 外科植入物金属材料第5部分:可锻钴铬钨镍合金 | Implants for surgery-Metallic materials-Part 5:Wrought cobaltchromium-tungsten-nickel alloy |
KS P ISO 5832-6-2007 | 外科植入物金属材料第6部分:可锻钴镍铬钼合金 | Implants for surgery-Metallic materials-Part 6:Wrought cobalt-nickel-chromium-molybdenum alloy |
KS P ISO 5832-7-2007 | 外科植入物金属材料第7部分:可锻和冷成形钴铬镍钼铁合金 | Implants for surgery-Metallic materials-Part 7:Forgeable and cold-formed cobalt-chromium-nickel-molybdenm-iron alloy |
KS P ISO 5832-8-2007 | 外科植入物金属材料第8部分:可锻钴镍铬钼钨铁合金 | Implants for surgery-Metallic materials-Part 8:Wrought cobaltnickel-chromium-molybdenum-tungsten-iron alloy |
KS P ISO 5832-9-2012 | 外科植入物金属材料第9部分:锻制高氮不锈钢 | Implants for surgery-Metallic materials-Part 9:Wrought high nitrogen stainless steel |
KS P ISO 5833-2012 | 外科植入物丙烯酸树脂粘合剂 | Implants for surgery-Acrylic resin cements |
KS P ISO 5834-1-2007 | 外科植入物超高分子量聚乙烯第1部分:粉末状 | Implants for surgery-Ultra-high-molecular-weight polyethylene-Part 1:Powder form |
KS P ISO 5834-2-2012 | 外科植入物超高分子量聚乙烯第2部分:成型模 | Implants for surgery-Ultra-high molecular weight polyethylene-Part 2:Moulded forms |
KS P ISO 5834-3-2008 | 外科植入物超高分子量聚乙烯第3部分:加速老化法 | Implants for surgery-Ultra-high-molecular-weight polyethylene-Part 3:Accelerated ageing methods |
KS P ISO 5834-4-2007 | 外科植入物超高分子量聚乙烯第4部分:氧化指数测量方法 | Implants for surgery-Ultra-high molecular weight polyethylene-Part 4:Oxidation index measurement method |
KS P ISO 5834-5-2007 | 外科植入物超高分子量聚乙烯第5部分:形态评定方法 | Implants for surgery-Ultra-high-molecular-weight polyethylene-Part 5:Morphology assessment method |
KS P ISO 5835-2008 | 外科植入物.六角传动连接的非对称螺纹球形头下金属骨螺钉.尺寸 | Implants for surgery-Metal bone screws with hexagonal drive connection, spherical under-surface of head, asymmetrical thread-Dimensions |
KS P ISO 5836-2010 | 外科植入物-金属骨板-与具有不对称螺纹和球形下表面的螺钉相对应的孔 | Implants for surgery-Metal bone plates-Holes corresponding to screws with asymmetrical thread and spherical under-surface |
KS P ISO 5837-1-2010 | 外科植入物.髓内钉系统.第1部分:立体或V形截面的髓内钉 | Implants for surgery-Intramedullary nailing systems-Part 1:Intramedullary nails with cloverleaf or V-shaped cross-section |
KS P ISO 5837-2-2010 | 外科植入物.髓内钉系统.第2部分:髓内钉 | Implants for surgery-Intramedullary nailing systems-Part 2:Medullary pins |
KS P ISO 5838-1-2009 | 外科植入物骨骼销和骨架丝第1部分:材料和机械要求 | Implants for surgery-Skeletal pins and wires-Part 1:Material and mechanical requirements |
KS P ISO 5838-2-2010 | 外科植入物骨骼销和骨架线第2部分:斯坦曼骨骼销尺寸 | Implants for surgery-Skeletal pins and wires-Part 2:Steinmann skeletal pins-Dimensions |
KS P ISO 5838-3-2010 | 外科植入物.骨骼针和骨骼线.第3部分:克什纳骨骼线 | Implants for surgery-Skeletal pins and wires-Part 3:Kirschner skeletal wires |
KS P ISO 5840-2007 | 心血管植入物-心脏瓣膜假体 | Cardiovascular implants-Cardiac valve prostheses |
KS P ISO 5841-2-2012 | 外科植入物心脏起搏器第2部分:脉冲发生器或导联人群临床性能报告 | Implants for surgery-Cardiac pacemakers-Part 2:Reporting of clinical performance of populations of pulse generators or leads |
KS P ISO 5841-3-2012 | 外科植入物心脏起搏器第3部分:可植入起搏器用低断面连接器(IS-1) | Implants for surgery-Cardiac pacemakers-Part 3:Low-profile connectors(IS-1) for implantable pacemakers |
KS P ISO 595-1 | 医用可重复使用的全玻璃或金属玻璃注射器第1部分:尺寸 | Reusable all-glass or metal-and-glass syringes for medical use-Part 1:Dimensions |
KS P ISO 595-2 | 医用可重复使用的全玻璃或金属玻璃注射器第2部分:设计、性能要求和试验 | Reusable all-glass or metal-and-glass syringes for medical use-Part 2:Design, performance requirements and tests |
KS P ISO 6161-2017 | 个人用护目镜.防激光辐射的滤光镜和护目镜 | Personal eye-protectors — Filters and eye-protectors against laser radiation |
KS P ISO 6360-1-2009 | 牙科.旋转器械的数字编码系统.第1部分:一般特性 | Dentistry-Number coding system for rotary instruments-Part 1:General characteristics |
KS P ISO 6360-2-2009 | 牙科旋转器械编号规则第2部分:形状 | Dentistry-Number coding system for rotary instruments-Part 2:Shapes |
KS P ISO 6360-3-2009 | 牙科学旋转器械的数字编码系统第3部分:牙钻和切割器的特殊特性 | Dentistry-Number coding system for rotary instruments-Part 3:Specific characteristics of burs and cutters |
KS P ISO 6360-4-2009 | 牙科旋转器械的数字编码系统第4部分:金刚石器械的特殊特性 | Dentistry-Number coding system for rotary instruments-Part 4:Specific characteristics of diamond instruments |
KS P ISO 6360-5-2009 | 牙科旋转器械的数字编码系统第5部分:根管器械的特殊特性 | Dentistry-Number coding system for rotary instruments-Part 5:Specific characteristics of root-canal instruments |
KS P ISO 6360-6-2009 | 牙科旋转器械的数字编码系统第6部分:磨具的特殊特性 | Dentistry-Number coding system for rotary instruments-Part 6:Specific characteristics of abrasive instruments |
KS P ISO 6360-7-2009 | 牙科旋转器械的数字编码系统第7部分:芯轴和专用器械的特殊特性 | Dentistry-Number coding system for rotary instruments-Part 7:Specific characteristics of mandrels and special instruments |
KS P ISO 6474-2009 | 外科植入物高纯氧化铝陶瓷材料 | Implants for surgery-Ceramic materials based on high purity alumina |
KS P ISO 6475-2010 | 外科植入物.不对称螺纹和球形下表面的金属接骨螺钉.机械性能要求和试验方法 | Implants for surgery-Metal bone screws with asymmetrical thread and spherical under-surface-Mechanical requirements and test methods |
KS P ISO 6710-2009 | 一次性使用静脉血样采集容器 | Single-use containers for venous blood specimen collection |
KS P ISO 6872-2009 | 牙科陶瓷材料 | Dentistry-Ceramic materials |
KS P ISO 6873-2014 | 牙科.石膏制品 | Dentistry — Gypsum products |
KS P ISO 6874-2009 | 牙科用聚合物基坑缝密封剂 | Dentistry-Polymer-based pit and fissure sealants |
KS P ISO 6876-2014 | 齿根管密封材料 | Dentistry — Root canal sealing materials |
KS P ISO 6877-2013 | 牙科学牙根管充填点 | Dentistry-Root-canal obturating points |
KS P ISO 7151-2008 | 外科器械.非切割铰接器械.一般要求和试验方法 | Surgical instruments-Non-cutting, articulated instruments-General requirements and test methods |
KS P ISO 7153-1-2018 | 外科器械材料第1部分:金属 | Surgical instruments ─ Materials ─ Part1: Metals |
KS P ISO 7176-1-2018 | 轮椅.第1部分:静态稳定性的测定 | Wheelchairs-Part 1:Determination of static stability |
KS P ISO 18192-1-2009 | 轮椅第10部分:电动轮椅爬障碍能力的测定 | Wheelchairs-Part 10:Determination of obstacle-climbing ability of electrically powered wheelchairs |
KS P ISO 20776-1-2009 | 轮椅.第11部分:试验假人 | Wheelchairs-Part 11:Test dummies |
KS P ISO 20776-2-2009 | 轮椅第13部分:试验表面摩擦系数的测定 | Wheelchairs-Part 13:Determination of coefficient of friction of test surfaces |
KS P ISO 20795-1-2014 | 轮椅.第14部分:电动轮椅和踏板车的动力和控制系统.要求和试验方法 | Wheelchairs — Part 14: Power and control systems for electrically powered wheelchairs and scooters — Requirements and test methods |
KS P ISO 20795-2-2011 | 轮椅第15部分:信息披露、文件编制和标签要求 | Wheelchairs-Part 15:Requirements for information disclosure, documentation and labelling |
KS P ISO 21672-1-2018 | 轮椅.第16部分:姿势支撑装置的耐点燃性 | Wheelchairs — Part 16: Resistance to ignition of postural support devices |
KS P ISO 21672-2-2018 | 轮椅.第19部分:汽车座椅用轮式移动装置 | Wheelchairs — Part 19: Wheeled mobility devices for use as seats in motor vehicles |
KS P ISO 7176-2-2011 | 轮椅第2部分:电动轮椅动态稳定性的测定 | Wheelchairs-Part 2:Determination of dynamic stability of electric wheelchairs |
KS P ISO 22442-1-2017 | 轮椅第21部分:电动轮椅、摩托车和蓄电池充电器的电磁兼容性要求和试验方法 | Wheelchairs-Part 21:Requirements and test methods for electromagnetic compatibility of electrically powered wheelchairs and scooters, and battery chargers |
KS P ISO 22442-2-2017 | 轮椅.第22部分:设置程序 | Wheelchairs — Part 22: Set-up procedures |
KS P ISO 24415-1-2011 | 轮椅第25部分:电动轮椅用蓄电池和充电器 | Wheelchairs ─ Part 25: Batteries and chargers for powered wheelchairs |
KS P ISO 24415-2-2012 | 轮椅.第26部分:词汇 | Wheelchairs-Part 26:Vocabulary |
KS P ISO 7176-3-2017 | 轮椅.第3部分:制动器效能的测定 | Wheelchairs-Part 3:Determination of effectiveness of brakes |
KS P ISO 7176-4-2018 | 轮椅.第4部分:理论距离范围测定用电动轮椅和踏板车的能耗 | Wheelchairs — Part 4: Energy consumption of electric wheelchairs and scooters for determination of theoretical distance range |
KS P ISO 7176-5-2011 | 轮椅第5部分:尺寸、质量和操纵空间的测定 | Wheelchairs-Part 5:Determination of dimensions,mass and manoeuvring space |