共找到 1850 条与 眼科设备 相关的标准,共 124 页
Inventory management specification for contact lenses
本文件规定了接触镜护理产品中保湿润滑剂(羟丙基甲基纤维素和聚乙烯吡咯烷酮)含量的测定方法。本文件适用于含保湿润滑剂(羟丙基甲基纤维素和/或聚乙烯吡咯烷酮)的接触镜护理产品。
Ophthalmic optical contact lens care products Part 10: Method for determination of moisturizing lubricants
本文件规定了用于观察眼底间接像的手持式、眼镜式、头戴式间接检眼镜的最低要求和试验方法。本文件适用于手持式、眼镜式、头戴式间接检眼镜。本文件不适用于间接检眼镜用的聚光镜和附件。本文件不适用于台面固定式的仪器,也不适用于主要用于图像捕捉和/或图像处理的检眼镜,如采用扫描激光技术的检眼镜。
Ophthalmic Instrument Indirect Ophthalmoscope
本文件规定了眼科激光光凝仪的术语和定义、产品组成、要求、试验方法等内容。本文件适用于临床上进行眼底激光光凝治疗的设备。
Laser treatment equipment Ophthalmic laser photocoagulation device
本文件规定了接触镜护理产品的安全和性能要求。
Ophthalmic optical contact lens care products Part 2: Basic requirements
本文件规定了定制太阳镜和太阳镜片的定义、要求、试验方法、标志、包装、运输和储存。 本文件适用于一般用途的定制太阳镜和太阳镜片,包括基片着色和膜层着色的太阳镜片。 本文件不适用于防护人造光源(如日光浴室使用的光源)辐射的镜片和用于工业用途的护目镜,也不适用于可直接观测太阳(如观测日蚀等)的特殊镜片。
Custom Sunglasses and Sunglasses
本文件规定了蓝光防护成镜和蓝光防护镜片的术语和定义、要求、试验方法、标志等。 本文件适用于光透射比大于80%(0类)的蓝光防护成镜和蓝光防护镜片。
Blue Light Protective Mirrors and Lenses
BS EN 80601-2-58. Medical electrical equipment - Part 2-58. Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery
1 Scope This document, together with ISO 15004‑1 and ISO 15004‑2, specifies minimum requirements and test methods for hand-held direct ophthalmoscopes designed for directly observing the eye fundus. This document takes precedence over ISO 15004‑1 and ISO 15004‑2, if differences exist.
Ophthalmic instruments. Direct ophthalmoscopes
1 Scope This document is applicable to ophthalmic viscosurgical devices (OVDs), a class of surgical invasive medical devices with viscous and/or viscoelastic properties, intended for use during surgery in the anterior segment of the human eye. OVDs are designed to create and maintain space, to protect intraocular tissues and to manipulate tissues during surgery. This document specifies requirements with regard to safety for the intended performance, design attributes, preclinical and clinical evaluation, sterilization, product packaging, product labelling and information supplied by the manufacturer of these devices.
Ophthalmic implants. Ophthalmic viscosurgical devices
1 Scope This document specifies requirements for the transmittance properties of uncut and unmounted finished spectacle lenses, including attenuation of solar radiation. This document is not applicable to — spectacle lenses having specific transmittance or absorption characteristics prescribed for medical reasons, — products to which specific personal protective equipment transmittance standards apply, and — products intended for direct observation of the sun, such as for solar-eclipse viewing. NOTE 1 By reference to ISO 21987 and ISO 14889, this document also applies to lenses mounted in spectacles. NOTE 2 Optical and geometric requirements are given for uncut finished spectacle lenses in ISO 8980‑1 and ISO 8980‑2, and for mounted lenses, in ISO 21987.
Ophthalmic optics. Uncut finished spectacle lenses. Transmittance specifications and test methods
This document specifies requirements for the transmittance properties of uncut and unmounted finished spectacle lenses, including attenuation of solar radiation. This document is not applicable to — spectacle lenses having specific transmittance or absorption characteristics prescribed for medical reasons, — products to which specific personal protective equipment transmittance standards apply, and — products intended for direct observation of the sun, such as for solar-eclipse viewing. NOTE 1 By reference to ISO 21987 and ISO 14889, this document also applies to lenses mounted in spectacles. NOTE 2 Optical and geometric requirements are given for uncut finished spectacle lenses in ISO 8980‑1 and ISO 8980‑2, and for mounted lenses, in ISO 21987.
Ophthalmic optics - Uncut finished spectacle lenses - Part 3: Transmittance specifications and test methods (ISO 8980-3:2022)
Ophthalmic instrument fundus camera
This document specifies requirements for the transmittance properties of uncut and unmounted finished spectacle lenses, including attenuation of solar radiation. This document is not applicable to — spectacle lenses having specific transmittance or absorption characteristics prescribed for medical reasons, — products to which specific personal protective equipment transmittance standards apply, and — products intended for direct observation of the sun, such as for solar-eclipse viewing. NOTE 1 By reference to ISO 21987 and ISO 14889, this document also applies to lenses mounted in spectacles. NOTE 2 Optical and geometric requirements are given for uncut finished spectacle lenses in ISO 8980-1
Ophthalmic optics — Uncut finished spectacle lenses — Part 3: Transmittance specifications and test methods
BS EN ISO 9342-1. Optics and optical instruments. Test lenses for calibration of focimeters - Part 1. Reference lenses for focimeters used for measuring spectacle lenses
Ophthalmic Optical Contact Lens Care Products Part 5: Determination of Physical Compatibility of Contact Lenses and Contact Lens Care Products
Medical electrical equipment - Part 2-58: Particular requirements for basic safety and essential performance of lens extraction and vitrectomy equipment for ophthalmic surgery
Hygienic handling of ophthalmic optical contact lenses when multiple patients try on contact lenses
ISO 11979-2:2014 specifies requirements and test methods for certain optical properties of intraocular lenses (IOLs) with any of spherical, aspheric, monofocal, toric, multifocal, and/or accommodative optics. The generic descriptor ?IOL' used throughout ISO 11979-2:2014 also includes phakic intraocular lenses (PIOL).
Ophthalmic implants — Intraocular lenses — Part 2: Optical properties and test methods
This document is applicable to ophthalmic viscosurgical devices (OVDs), a class of surgical invasive medical devices with viscous and/or viscoelastic properties, intended for use during surgery in the anterior segment of the human eye. OVDs are designed to create and maintain space, to protect intraocular tissues and to manipulate tissues during surgery. This document specifies requirements with regard to safety for the intended performance, design attributes, preclinical and clinical evaluation, sterilization, product packaging, product labelling and information supplied by the manufacturer of these devices.
Ophthalmic implants - Ophthalmic viscosurgical devices (ISO 15798:2022)
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