C36 其他专科器械 标准查询与下载

CSA C22.2 No.60601.2.36-98-1998 医疗电气设备-第2部分:体外感应碎石机安全的特殊要求.第1版.通用指令第1号

Ce document constitue Ia premiere edition de Ia norme CAN/CSA-C22.2 n° 60601 .2.36, Apparel/s électromédicaux — Partie 2 Règles particulières de sécurité des apparel/s pour lit hot ritie créée de ía con extra-corporelle. Elle fait partie d'une série de

Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Equipment for Extracorporeally Induced Lithotripsy First Edition; General Instruction No 1

CSA CEI-C22.2NO60601.2.36CAN/-1998 医疗电气设备-第2部分:体外碎石仪的安全特殊要求.第1版.通用指令第1号.CEI 60601-2-36:1997.该标准应与CAN/CSA-C标准一起使用

Appareils Electromedicaux - Partie 2: Regles Particulieres De Securite Des Appareils Pour Lithotritie Creee De Facon Extra-Corporelle Premiere Edition; Fiche No 1; CEI 60601-2-36: 1997; Cette Norme Doit Etre Utilisee Conjointement Avec La Norme CAN/CSA-C

Medical Electrical Equipment-Part 2: Particular Requirements for the Safety of In Vitro Lithotriptic Device.First Edition.General Instruction No 1.CEI 60601-2-36:1997.The Standard shall be used with CAN/CSA-C Standard together

CSA C22.2 No.601.2.31-98-1998 医疗电气设备-第2部分:具有内部功率源的外部心脏起搏器安全的特殊要求.第1版.更正1:2001.CEI 601-2-31:1994

Although the intended primary application of this Standard is stated in its Scope, it is important to note that it remains the responsibility of the users of the Standard to judge its suitability for their particular purpose.

Appareils Electromedicaux - Partie 2: Regles Particulieres De Securite Des Stimulateurs Cardiaques Externes A Source D'Energie Interne Premiere Edition; Modification 1:2001; CEI 601-2-31: 1994

CSA C22.2 No.601.2.21-98-1998 医疗电气设备-第2部分:新生儿辐射保育器安全的特殊要求.第1版.更正1:2001.CEI 601-2-21:1994

Appareils Electromedicaux - Partie 2: Regles Particulieres De Securite Des Incubateurs Radiants Pour Nouveau-Nes Premiere Edition; Modification 1:2001; CEI 601-2-21: 1994

Appareils Electromedicaux - Partie 2: Regles Particulieres De Securite Des Incubateurs Radiants Pour Nouveau-Nes Premiere Edition; Modification 1:2001; CEI 601-2-21: 1994

CSA CEI-1289-2-98-CAN/CSA-1998 高频电流电子外科仪-第2部分:维修.第1版.CEI/IEC 1289-2:1994

Appareils D´Electrochirurgie A Courant Haute Frequence - Partie 2: Maintenance Premiere Edition; CEI/IEC 1289-2: 1994

Appareils D碋lectrochirurgie A Courant Haute Frequence - Partie 2: Maintenance Premiere Edition; CEI/IEC 1289-2: 1994

CSA CEI-1288-2-98-CAN/CSA-1998 心脏除颤器-心脏除颤器监视器-第2部分:维修.第1版.CEI/IEC 1288-2:1993

Defibrillateurs Cardiaques - Moniteurs-Defibrillateurs Cardiaques - Partie 2: Maintenance Premiere Edition; CEI/IEC 1288-2: 1993

Defibrillateurs Cardiaques - Moniteurs-Defibrillateurs Cardiaques - Partie 2: Maintenance Premiere Edition; CEI/IEC 1288-2: 1993

CSA ISO-10993.3-97-CAN/CSA:1997 医疗器械生物学评价 第3部分：有关基因毒性、致癌性和生殖毒性的测试 第一版

This standard applies to the following electronic flash apparatus for photographic purposes, having a stored energy not exceeding 2000 J, together with associated apparatus and not intended to be subjected to dripping or splashing:

Biological Evaluation of Medical Devices - Part 3: Tests Concerning Genotoxicity, Cancerogenicity and Reproductive Toxicity First Edition

CSA ISO 10993.4-97-CAN/CSA:1997 医疗器械生物学评价 第4部分：与血液相互作用的试验选择第一版； ISO 10993-4:1992

L'Association canadienne de normalisation (CSn), sous les auspices de laquelle ceite Norme nationale a été préparée, a re?u ses lettres patentes en 1919 et son accréditation au sein du Systbme de normes nationales par le Conseil canadien des normes en 19

Biological evaluation of medical devices - Part 4: Choice of tests concerning interactions with blood The First Edition; ISO 10993-4:1992

CSA ISO-10993.4-97-CAN/CSA:1997 医疗器械生物学评估-第4部分:与血液相互作用试验选择

This Standard applies to track ystems with two or more poles for the connection of luminaires to the electrical supply, either of rated voltage not exceeding 300 V between poles, 150 Volts-to-ground with the provision for earthing (Class I) and a minimu

Evaluation Biologique Des Dispositifs Medicaux - Partie 4: Choix Des Essais Concernant Les Interactions Avec Le Sang

BS ISO 11948-1:1997 吸尿工具.第1部分:整体试验

This part of ISO 11948 specifies a method for determining the absorption capacity of the absorbent core of body-worn urine-absorbing aids. NOTE —Other methods for measuring absorption capacity examine aspects which are outside the scope of this part of ISO 11948.

Urine-absorbing aids - Whole-product testing

DOD MIL-F-89018 NOTICE 1-1997 高程数据火灾寻视器(FFED)

This notice should be filed in front of MIL-F-89018, dated 1 October 1992.

FIREFINDER ELEVATION DATA (FFED)

CSA Z168.5.6-96-CAN/CSA-1996 肺部呼气用人工呼吸器.第1版本.通用指令第1号

A reference comparison method. This method is applicable to two character strings to determine their relative order. The method can be applied to strings containing characters from the full repertoire of ISO/IEC 10646-1. This method is also applicable t

Reanimateurs A Air Expire; Technologie Des Soins Medicaux Premiere Edition; Fiche No 1

DOD A-A-55711-1996 血浆冷藏

This Commercial Item Description covers an undercounter,blood plasma freezer.

FREEZER, UNDER COUNTER, BLOOD PLASMA

YY/T 0245.2-1996 管型消化道吻合器

本标准规定了管型消化道吻合器的产品分类、技术要求等。 本标准适用于管型消化道吻合器，该产品供消化道手术吻合用。

Tubular Gastrointestinal Stapler

ARMY MIL-M-12971 B NOTICE 2-1996 M1瓣膜置换机

Thisnotice should be filed in front of MIL-M-12971B(MU) dated 23 May 1966.

MECHANISM, VALVE REPLACEMENT, M1

BS EN 61266:1995 超声波 手持式探头胎儿多普勒心跳检测器 性能要求以及测量和报告方法

Applies to detectors which generate a single continuous wave or quasi-continuous wave ultrasonic beam. It does not cover continuous monitoring devices which generate more than one ultrasound beam and use a flat standard probe strapped to a patient. This standard is not an equipment design standard.

Ultrasonics. Hand-held probe Doppler foetal heartbeat detectors. Performance requirements and methods of measurement and reporting

JIS T 1603:1995 人工心肺的电动血液泵

この規格は，主に開心術中の生命維持を目的とした血液の体外循環機能をもつ人工心肺装置の血液ポンプのうち，電動機を動力源とするローラ形の血液ポンプ（以下，血液ポンプという。)について規定する。

Electric motor driven blood pump for cardiopulmonary bypass

DOD A-A-55699-1995 病人监测器

This Commercial Item Description covers a patient monitor for use in vital signs monitoring indoors, outdoors, and during transport.

PATIENT MONITOR

DOD A-A-54981-1995 便携式适度调节器(治疗学的)

The following National Stock Number is covered by this document.

HUMIDIFIER, PORTABLE (THERAPEUTIC)

YY/T 0184-1994 输精管分离钳

本标准规定了输精管分离钳的型式，技术要求、试验方法、检验规则和标志、包装、运输、贮存等要求。 本标准适用于输精管分离钳．该产品供输精管直视钳穿和注射粘堵手术时作分离阴囊皮肤、剥离提取输精管、压挫输精管结扎部位和钳夹精膜进行隔离包埋近睾残端用，必要时可作止血用。

Separating pliers for spermaduct