C40 医用光学仪器设备与内窥镜 标准查询与下载



共找到 284 条与 医用光学仪器设备与内窥镜 相关的标准,共 19

本标准规定了食管窥镜的定义及分类、要求、试验方法、检验规则、标志、使用说明书、包装、运输和贮存的要求。 本标准适用于医疗临床使用的食管窥镜(以下简称窥镜),窥镜主要适用于食管病变的检查和/或与手术器械配合进行病变部位的治疗。

Esophagoscope

ICS
11.040
CCS
C40
发布
2008-04-25
实施
2009-12-01

YY 0068的本部分规定了硬性内窥镜光学性能要求、试验方法。 本部分适用于医疗目的的硬性内窥镜。

Medical Endoscopes.Rigid Endoscope.Part 1:Optical properties and test methods

ICS
11.040
CCS
C40
发布
2008-04-25
实施
2009-12-01

Ophthalmic instruments—Indirect ophthalmoscopes

ICS
11.040
CCS
C40
发布
2008-04-25
实施
2009-12-01

이 규격은 의과에서 사용하는 위경에 대하여 규정한다.

Gastroscopes

ICS
11.040.30
CCS
C40
发布
2007-10-04
实施
2007-10-04

이 규격은 의료에 사용하는 방광경에 대하여 규정한다.

Cystoscopes

ICS
11.040.00
CCS
C40
发布
2007-10-04
实施
2007-10-04

ERRATUM

ICS
CCS
C40
发布
2007-09-12
实施

本标准规定了硬性宫腔内窥镜的分类和标记、要求、试验方法、检验规则、标志、标签和使用说明书、包装、运输、贮存。 本标准适用于硬性宫腔内窥镜(以下简称宫腔镜)。宫腔镜主要用于医学临床中对子宫腔疾病的诊断和配合手术器械进行治疗。 本标准不适用于高频电切宫腔镜。

Rigid hysteroscope

ICS
11.040.70
CCS
C40
发布
2007-07-02
实施
2008-03-01

本标准规定了硬性关节内窥镜的分类和标记、要求、试验方法、检验规则、标志、标签和使用说明书、包装、运输、贮存。 本标准适用于硬性关节内窥镜(以下简称关节镜),关节镜适用于医学临床中对人体关节疾病的检查、诊断,配合相关手术系统可进行治疗。

Rigid arthroscope

ICS
11.040.70
CCS
C40
发布
2007-07-02
实施
2008-03-01

本标准规定了纤维大肠内窥镜的分类和标记、要求、试验方法、检验规则、标志、使用说明书和包装、运输、贮存。 本标准适用于纤维大肠内窥镜(以下简称纤维大肠镜)。该产品用于人体大肠内腔的检查、诊断,配合相关手术系统可进行治疗。

Large intestine fiber endoscope

ICS
11.040.70
CCS
C40
发布
2007-07-02
实施
2008-03-01

本标准规定了硬性电凝切割内窥镜的分类和标记、要求、试验方法、检验规则、标志、标签和使用说明书、包装、运输、贮存。 本标准适用于硬性电凝切割内窥镜(以下简称电切镜)。电切镜适用于临床医疗检查,并利用高频电流热效应对病变组织进行切割、凝血等手术。

Rigid resectosocope

ICS
11.040.70
CCS
C40
发布
2007-07-02
实施
2008-08-01

Ophthalmic instruments - Slit-lamp microscopes.

ICS
11.040.70
CCS
C40
发布
2007-05-01
实施
2007-05-05

Ophthalmic optics - Definitions and symbols of spectacle lenses in connection with the human eye

ICS
11.040.70
CCS
C40
发布
2007-05
实施

This International Standard, together with ISO 15004-1 and ISO 15004-2, specifies requirements and test methods for slit-lamp microscopes to provide slit illumination and observation under magnification of the eye and its adnexa. This International Standard is not applicable to microscope accessories, e.g. photographic equipment and lasers. This International Standard takes precedence over ISO 15004-1 and ISO 15004-2, if differences exist.

Ophthalmic instruments - Slit-lamp microscopes (ISO 10939:2007); English version of DIN EN ISO 10939:2007-04

ICS
11.040.70
CCS
C40
发布
2007-04
实施

This standard applies any intraocular lens implant whose primary indication is the correction of aphakia and whose optic is designed to provide simultaneous distance and near vision. For the purposes of this standard, these implants are referred to as mu

Multifocal Intraocular Lenses

ICS
11.040.70
CCS
C40
发布
2007-03-26
实施

Ophthalmic instruments - Indirect ophthalmoscopes.

ICS
11.040.70
CCS
C40
发布
2007-03-01
实施
2007-03-20

Ophthalmic instruments - Direct ophthalmoscopes.

ICS
11.040.70
CCS
C40
发布
2007-03-01
实施
2007-03-20

本标准规定了微循环显微镜的术语和定义、分类和标记、要求、试验方法、检验规则、标志与使用说明书、包装、运输、贮存。 本标准适用于各种类型的微循环显微镜,该类产品用于体表微循环的观察。

Micro-circulation microscopes

ICS
11.040.70
CCS
C40
发布
2007-01-31
实施
2008-02-01

本标准规定了准分子激光角膜屈光治疗机的术语和定义、结构和基本参数、要求、试验方法、检验规则、标志、包装、运输、贮存。 准分子激光角膜屈光治疗机(以下简称治疗机)主要用于屈光性角膜切削术(PRK)、原位角膜磨镶术(LASIK)等角膜屈光矫正术和治疗性角膜切削术(PPK)。

Excimer laser cornea ametropia cure system

ICS
11.040.70
CCS
C40
发布
2007-01-31
实施
2008-02-01

本标准规定了裂隙灯显微镜的适用范围、定义、要求、试验方法、检验规则、标志、包装、运输和贮存。 本标准适用于裂隙灯显微镜,该产品供检查眼前节及眼内部病变用。

Ophthalmic instruments Slit-lamp microscopes

ICS
11.040.70
CCS
C40
发布
2007-01-31
实施
2008-02-01

The purpose of this Technical Report is to explain the changes relating to power measurements in the revised editions of ISO 8980-1 [6] and ISO 8980-2 [7]. In order to illustrate the issues raised, an inter-laboratory power measurement study was conducted on ten different lenses measured by nine organizations worldwide. Twenty-five focimeters of different types were used. The test lenses were spherically powered allyl diglycol carbonate (ADC)1) hard resin lenses surfaced to –4,00 D, –2,00 D, 0,00 D, +2,00 D, and +4,00 D, each with an addition power of 2,50 D. Five were D28 bifocals and five were progressive power lenses. The measurements were front distance power, front near power, back distance power and back near power, for each lens and for each focimeter used. Each lens was measured nine times: five measurements taken without repositioning the lens and four measurements taken with the lens repositioned each time. The assessed parameters were divided into three categories: discrepancies due to focimeter design and measurement methods; systematic errors; random errors. For each parameter, experimental results are given, as well as theoretical ones when needed. Measurement data include front distance portion power, front near portion power, back distance portion power and back near portion power. NOTE The results of all measurements are available on the ISOTC Server at the address given in the Bibliography[8]. Unless stated otherwise, in order to show relevant information, the results shown are for the D28 bifocals when no different behaviour was found for the progressive power lenses.

Ophthalmic optics - Spectacle lenses - Parameters affecting lens power measurement

ICS
CCS
C40
发布
2007-01
实施



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