共找到 1323 条与 一般与显微外科器械 相关的标准,共 89 页
Intravascular catheters—Sterile and single-use catheters—Part 5:Over-needle peripheral catheters
Sterile, single-use intravascular catheters
Sterile single use anesthesia filters for use with epidural catheter
This document specifies requirements and test methods for single-use receptacles, intended by their manufacturer, for the collection of venous blood specimens derived from the human body, for the purposes of in vitro diagnostic examination. This document also applies to receptacles containing media for blood culture.
Single-use containers for human venous blood specimen collection (ISO 6710:2017); German version EN ISO 6710:2017
The project defines dimensions and marking of scissors type Joseph, angled to side, as used in surgery, public health service or armed forces. The project defines dimensions and marking of scissors type Joseph, angled to side, as used in surgery and public health service.
Medical instruments - Scissors type Joseph
The project defines dimensions and marking of tissue forceps type Adson-Brown, angled to side, as used in surgery and public health service.
Medical instruments - Tissue forceps type Adson-Brown
The project defines dimensions and marking of scissors for preparations without carbide inserts, as used in surgery and public health service.
Medical instruments - Part 1: Scissors for preparations without carbide inserts
Sterile single-use catheter introducers
Standardization of dimensions, material, requirements, designation and marking of the vessel forceps type De Bakay for use in surgery.
Medical instruments - Vessel forceps type De Bakey
The project defines dimensions and marking of scissors type Kilner, angled to side, as used in surgery, public health service.
Medical instruments - Scissors type Kilner
Introducer needles and introducer catheters
This document specifies the material, performance requirements and labelling and gives recommendations for shape and dimensions of plunger stoppers for pen-injectors for medical use. NOTE The potency, purity, stability and safety of a medicinal product during its manufacture and storage can strongly be affected by the nature and performance of the primary packaging.
Pen systems - Part 2: Plunger stoppers for pen-injectors for medical use
This document defines dimensions and marking of surgical scissors, straight without carbide inserts, angled to side, as used in surgery and public health service.
Medical instruments - Part 1: Surgical scissors, straight without carbide inserts
This document defines dimensions and marking of scissors for incisions, as used in public health Service.
Medical instruments - Scissors for incisions
This part of EN ISO 10555 specifies requirements, performance, and user safety issues related to subcutaneous implanted ports and catheters for intravascular long-term use supplied in sterile condition and intended for single use.This part of EN ISO 10555 does not specify requirements, performance, and user safety issues related to non-coring needles.
Intravascular catheters - Sterile and single-use catheters - Part 6: Subcutaneous implanted ports (ISO 10555-6:2015); German version EN ISO 10555-6:2017
Optics and photonics. Operation microscopes. Requirements and test methods
This part of ISO 8536 specifies the shape, dimensions, material, performance requirements and labelling for the type of closure for infusion bottles, as described in ISO 8536-1, that is used in connection with the freeze-drying (or lyophilization) of drugs and biological materials. The dimensional requirements are not applicable to barrier-coated closures. Closures specified in this document are intended for single use only. Freeze drying closures can pick up water during shipping, storage, washing and steam sterilization cycles, which is difficult to remove in a subsequent drying cycle. As a consequence, the freeze drying closures are usually loaded with residual moisture. Depending upon the mass of the freeze-dried product and the degree of its sensitivity to water, the residual moisture in the rubber material can spoil the freeze-dried preparation during storage. These specific process requirements have been addressed in this part of ISO 8536 by specifying relevant requirements for freeze drying closures including a test method on determination of residual moisture.
Infusion equipment for medical use - Part 6: Freeze drying closures for infusion bottles (ISO 8536-6:2016)
Copyright ©2007-2022 ANTPEDIA, All Rights Reserved
京ICP备07018254号 京公网安备1101085018 电信与信息服务业务经营许可证:京ICP证110310号