11.040.55 诊断设备 标准查询与下载

AS ISO 7376.2:2002 给水用1/2 In.(12 mm)到2 In.(50 mm)聚乙烯-铝-聚乙烯和交联聚乙烯-铝-交联聚乙烯复合压力管

Specifies requirements for screw threads for miniature electric lamps and lamp sockets used in laryngoscopic blades to allow engagement, lamp illumination and disengagement through multiple cycles.

Laryngoscopic fittings - Miniature electric lamps - Screw threads and sockets for conventional blades

AS ISO 7376.3:2002 给水用1/2 In.(12 mm)到2 In.(50 mm)聚乙烯-铝-聚乙烯和交联聚乙烯-铝-交联聚乙烯复合压力管

Specifies basic dimensions and performance requirements for two designs of hook-on type fibre-illuminated re-usable rigid laryngoscopes.

Laryngoscopic fittings - Fibre-illuminated re-usable rigid laryngoscopes

DIN EN 60601-2-18:2001 医疗电气设备.第2-18部分:内窥设备安全性特殊要求

Medical electrical equipment - Part 2-18: Particular requirements for the safety of endoscopic equipment (IEC 60601-2-18:1996 + A1:2000); German version EN 60601-2-18:1996 + A1:2000

BS EN 60601-2-47:2001 医用电气设备.安全性专门要求.流动心电图测试系统特定安全要求(包括基本性能)

To be read in conjunction with BS EN 60601-1:1990

Medical electrical equipment - Particular requirements for safety - Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems

BS EN 60601-2-49:2001 医疗用电气设备.多功能病人监测设备安全的专门要求

This Particular Standard applies to the safety requirements of MULTIFUNCTION PATIENT MONITORING EQUIPMENT as defined in subclause 2.2.101. The scope of this standard is restricted to EQUIPMENT having either more than one APPLIED PART or more than one SINGLE FUNCTION, intended for connection to a single PATIENT. This standard does not specify requirements for individual monitoring functions.

Medical electrical equipment - Particular requirements for safety - Particular requirements for the safety of multifunction patient monitoring equipment

DS/EN 60601-2-18/A1:2001 医用电气设备 第2部分：内窥镜设备安全的特殊要求

This particular standard specifies requirements for the safety of endoscopic equipment and integrated instrumentation used for medical diagnosis and therapy and for treatment in body cavities. It is subdivided into five applications concerning endoscopes for (a) direct visualization, (b) integration with thermocautery or (c) lithotrite, (d) electrosurgery and (e) other specialized endoscopes.

Medical electrical equipment - Part 2: Particular requirements for the safety of endoscopic equipment

DIN EN 60601-2-34:2001 医疗电气设备.第2-34部分:侵入式血压监测仪器安全性(包括基本性能)的特殊要求

Medical electrical equipment - Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment (IEC 60601-2-34:2000); German version EN 60601-2-34:2000

DS/EN 60601-2-34:2001 医用电气设备 第 2-34 部分：有创血压监测设备的特殊安全要求，包括基本性能

This Particular Standard applies to INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT and MEASURING EQUIPMENT as defined in 2.101, hereinafter referred to as EQUIPMENT. This Particular Standard does not apply to catheter tubing, catheter needles, Luer locks, taps and tap tables. This Particular Standard also does not apply to non-invasive blood pressure monitoring equipment.

Medical electrical equipment - Part 2-34: Particular requirements for safety, including essential performance, of invasive blood pressure monitoring equipment

IEC 60601-2-49:2001 医用电气设备 第2-49部分：多功能病人监护设备安全的特殊要求

This Particular Standard applies to the safety requirements of MULTIFUNCTION PATIENT MONITORING EQUIPMENT as defined in subclause 2.2.101. The scope of this standard is restricted to EQUIPMENT having either more than one APPLIED PART or more than one SINGLE FUNCTION@ intended for connection to a single PATIENT. This standard does not specify requirements for individual monitoring functions.ObjectThe object of this Particular Standard is to specify requirements for the safety of MULTIFUNCTION PATIENT MONITORING EQUIPMENT.

Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment

IEC 60601-2-47:2001 医用电气设备 第2-47部分：不卧床的心电描记系统安全（包括主要性能）的特殊要求

Addition: This Particular Standard specifies the particular safety requirements for AMBULATORY ELECTROCARDIOGRAPHIC SYSTEMS, as defined in 2.101. Within the scope of this standard are systems of the following types: a) systems that provide continuous recording and continuous analysis of the ECG allowing full re-analysis giving essentially similar results. The systems may first record and store the ECG and analyse it later on a separate unit, or record and analyse the ECG simultaneously. The type of storage media used is irrelevant with regard to this standard; b) systems that provide continuous analysis and only partial or limited recording not allowing a full re-analysis of the ECG. The safety aspects of this standard apply to all types of systems falling in one of the above-mentioned categories. If the ambulatory electrocardiographic system offers automatic ECG analysis, minimal performance requirements for measurement and analysis functions apply. Medical electrical equipment covered by IEC 60601-2-25 and IEC 60601-2-27 are excluded from the scope of this standard. This standard does not apply to systems that do not continuously record and analyse the ECG (for example, 'intermittent event recorders').

Medical electrical equipment - Part 2-47: Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems

BS EN 60601-2-34:2001 医疗电气设备.安全性用特殊要求.直接血压监护设备安全性用特殊要求(包括基本性能)

To be read in conjunction with BS EN 60601-1:1990

Medical electrical equipment - Particular requirements for safety - Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment

DIN EN 60601-2-25:2001 医疗电气设备.第2-25部分:心电图安全性特殊要求

Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs (IEC 60601-2-25:1993 + A1:1999); German version EN 60601-2-25:1995 + A1:1999

DS/EN 60601-2-23:2001 医用电气设备 第 2-23 部分：经皮分压监测设备的安全性（包括基本性能）的特殊要求

This particular Standard specifies requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment, as defined in 2.101 and hereinafter referred to as EQUIPMENT, whether this EQUIPMENT is stand alone or part of a system. It applies to transcutaneous monitors used with adults, children and neonates and includes the use of these devices in foetal monitoring during birth.

Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partical pressure monitoring equipment

DIN ISO 8600-4:2001 光学和光学仪器.医用内窥镜和内窥镜附件.第4部分:插入部分最大宽度测定

The document specifies a methods of measurement of the maximum width of the insertion portion of medical endoscopes and certain endoscopic accessoires, using either millimetre or French size indication.#,,#

Optics and optical instruments - Medical endoscopes and endoscopic accessories - Part 4: Determination of maximum width of insertion portion (ISO 8600-4:1997)

LST EN 60601-2-23-2000 医疗电气设备 第 2-23 部分：经皮分压监测设备（IEC 60601-2-23:1999）的特殊安全要求，包括基本性能

Medical electrical equipment. Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment (IEC 60601-2-23:1999)

DIN EN 60601-2-23:2000 医疗电气设备.第2-23部分:经皮分压监护设备包括基本性能在内的安全性的特殊要求

Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment (IEC 60601-2-23:1999); German version EN 60601-2-23:2000

IEC 60601-2-34:2000 医用电气设备 第2-34部分:直接血压监护设备安全专用要求

Addition: This Particular Standard applies to INVASIVE BLOOD PRESSURE MONITORING and measuring equipment as defined in 2.101@ hereinafter referred to as EQUIPMENT. This Particular Standard does not apply to CATHETER tubing@ CATHETER needles@ Luer locks@ taps and tap tables. This Particular Standard also does not apply to NON-INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT.

Medical electrical equipment - Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment

BS EN 60601-2-30:2000 医用电气设备.安全性详细要求.自动循环非侵入式血压监视设备包括基本性能的安全性详细要求

Addition: This Particular Standard specifies requirements for the safety, including essential performance, of AUTOMATIC CYCLING NON-INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT as defined in 2.102, hereinafter referred to as EQUIPMENT. The EQUIPMENT may be attended or unattended. This Particular Standard does not apply to blood pressure measuring equipment which uses finger transducers or to semi-automatic blood pressure measuring equipment, typically in which each determination needs to be initiated manually.

Medical electrical equipment. Particular requirements for safety. Particular requirements for safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment

IEC 60601-2-18/AMD1:2000 医用电气设备 第2-18部分:内窥镜设备安全专用要求 修改1

This is Amendment 1 to IEC 60601-2-18-1996 (Medical electrical equipment -Part 2-18:Particular requirements for the safety of endoscopic equipment)

Medical electrical equipment - Part 2-18: Particular requirements for the safety of endoscopic equipment; Amendment 1

BS EN 60601-2-23:2000 医疗电气设备.经皮分压监测设备的安全性用特殊要求(包括基本性能)

Addition: This Particular Standard specifies requirements for the safety, including essential performance, of TRANSCUTANEOUS PARTIAL PRESSURE MONITORING EQUIPMENT, as defined in 2.101 and hereinafter referred to as EQUIPMENT, whether this EQUIPMENT is stand alone or part of a system. It applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth. It does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa).

Medical electrical equipment - Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment