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SNV - SN EN ISO 10555-1

Sterile, single-use intravascular catheters - Part 1: General requirements

inactive
Organization: SNV
Publication Date: 1 October 2009
Status: inactive
Page Count: 30
ICS Code (Syringes, needles and catheters): 11.040.25

Document History

SN EN ISO 10555-1
October 1, 2013
Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements
This part of ISO 10555 specifies general requirements for intravascular catheters, supplied in the sterile condition and intended for single use, for any application. It is not applicable to...
SN EN ISO 10555-1
October 1, 2009
Sterile, single-use intravascular catheters - Part 1: General requirements
A description is not available for this item.

References

This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
15223-1 - Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements
Published by ISO on July 1, 2021
This document specifies symbols used to express information supplied for a medical device. This document is applicable to symbols used in a broad spectrum of medical devices, that are available...
This document references:
ISO 80369-1 - Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements
Published by ISO on November 1, 2018
This document specifies general requirements for small-bore connectors, which convey liquids or gases in healthcare applications. These small-bore connectors are used in medical devices or...
This document references:
ISO 7886-1 - Sterile hypodermic syringes for single use — Part 1: Syringes for manual use
Published by ISO on May 1, 2017
This document specifies requirements and test methods for verifying the design of empty sterile single-use hypodermic syringes, with or without needle, made of plastic or other materials and intended...
This document references:
ISO 11137-1 - Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices AMENDMENT 2: Revision to 4.3.4 and 11.2
Published by ISO on November 1, 2018
A description is not available for this item.
This document references:
ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on August 15, 2006
Inclusions This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE Although the scope of this...
This document references:
ISO 3105 - Glass Capillary Kinematic Viscometers - Specifications and Operating Instructions
Published by ISO on January 1, 1994
This International Standard gives specifications and operating instructions for glass capillary viscometers widely used for the determination of kinematic viscosity of petroleum products by the...
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