11.100 实验室医学 标准查询与下载
共找到 753 条与 实验室医学 相关的标准，共 51 页
Criterion of collecting testing material in case samples
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Criterions of package storage conrey and submitting materials in case samples
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Methods of qualitative and quantitative analysis for chloroquinoline in case samples
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Methods of qualitative and quantitative analysis for amitriptyline,doxpin,trimipramine,clomipramine,imipramine in cases samples
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Methods of qualitative and quantitative analysis for strychnine,brucine in case samples
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Compiling rule of a report for physical and chemical examination
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Methods of qualitative and quantitative analysis for DDVP and trichorfon in case samples
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Methods of qualitative and quantitative analysis for diazapam and chlordiazepoxide in cases samples
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Methods of qualitative and quantitative analysis for chlorpromazine and promethazine and perphenazine in case samples
- ICS
- 11.100
- CCS
- A92
- 发布
- 1998-12-08
- 实施
- 1999-03-01
Standard Specification for Disposable Glass Serological Pipets
- ICS
- 11.100
- CCS
- 发布
- 1998-10-10
- 实施
Standard Specification for Serological Pipet, Disposable Plastic
- ICS
- 11.100
- CCS
- 发布
- 1998-10-10
- 实施
The international community has decided to make this standard available only in the English language version. It has been adopted as a National Standard of Canada on this basis. This National Standard of Canada is equivalent to International Standard ISo 10993-9:1994. 1 Scope This Technical Report aims to facilitate the design of test procedures which are used to evaluate the biological responses to degradation products released from medical devices. Following brief descriptions of each major class of material used for medical devices, this Technical Report focuses on the likely mechanisms of degradation of these materials when they are used in a biological service environment. Accelerated time and real-time degradation testing environments for devices and materials are suggested along with characterization techniques for the degradation products. Finally, an approach for identifying and quantifying degradation products obtained from explanted devices and tissues is proposed.
Biological evaluation of medical devices - Part 9: Degradation of materials related to biological testing
- ICS
- 11.100
- CCS
- 发布
- 1998-01-01
- 实施
La présente Norme nationale du Canada est équivalente à la Norme internationale ISO 10993-1:1992. 1 Domaine d'application La présente partie de l'ISO 10993 fournit des recommandations relatives: a) aux principes fondamentaux sur lesquels repose l'évaluation biologique des dispositifs médicaux; b) à la définition des classes de dispositifs, basées sur la nature et la durée de contact avec le corps humain; c) au choix des essais appropriés. L'ISO 10993 ne traite pas de l'essai des matériaux et dispositifs qui n'entrent pas directement ou indirectement en contact avec le corps du patient. Elle n'aborde pas non plus les risques biologiques dus aux défaillances mécaniques. Les autres partie de l'ISO 10993 concernent des essais spéficiques, comme indiqués dans l'avant-propos (voir A.2, article 1, Domaine d'application).
Biological evaluation of medical devices - Part 1: Guidelines for the selection of tests
- ICS
- 11.100
- CCS
- 发布
- 1998-01-01
- 实施
Standard Specification for Disposable Glass Culture Tubes
- ICS
- 11.100
- CCS
- 发布
- 1998-01-01
- 实施
This National Standard of Canada is equivalent to International Standard ISO 10993-5:1992. 1 Scope This part of ISO 10993 describes test methods to assess the in vitro cytotoxicity of medical devices. NOTE 1 The term medical devices corresponds to the definition given in ISo 10993-1 and covers medical materials as well as dental material and devices. The definition is in accordance with the CEN standard document. These methods specify the incubation of cultured cells either directly or through diffusion a) with extracts of the device, and/or b) in contact with a device. These methods are designed to determine the biological response of mammalian cells in vitro using appropriate biological parameters.
Biological evaluation of medical devices - Part 5: Tests for cytotoxicity: in vitro methods
- ICS
- 11.100
- CCS
- 发布
- 1997-06-30
- 实施
本标准规定了用微生物法测定微量青霉素的试验方法。 本标准适用于成品、清场后环境、设备及空气中微量青霉素的测定。最小检出量0.008u/mL。
Test methods of penicillin
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-06-09
- 实施
- 1997-10-01
本标准规定了用示波极谱测定尿中铅浓度的方法。 本标准适用于正常人、接触铅作业的工人和铅吸收或铅中毒治疗病人尿中铅浓度的测定。
Urine.Determination of lead.Oscillo-polarographic method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-01-11
- 实施
- 19970901
本标准规定了用血液荧光计测定血中锌原卟啉浓度的方法。 本标准适用于接触铅的工人血中锌原卟啉浓度的测定。
Blood.Determination of zinc protoporphyrin.Hematofluorometer method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-01-11
- 实施
- 19970901
本标准规定了分光光度法测定尿中肌酐浓度的方法。 本标准适用于接触有害物质的工人尿中肌酐浓度的测定。
Urine.Determination of creatinine.Spectrophotometric method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-01-11
- 实施
- 19970901
