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DIN EN ISO 11070

Sterile intravaskulaere Einfuehrungsinstrumente, Dilatatoren und Fuehrungsdraehte zur einmaligen Verwendung (ISO 11070:2014 + Amd 1:2018); Deutsche Fassung EN ISO 11070:2014 + A1:2018

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Organization: DIN
Publication Date: 1 April 2019
Status: active
Page Count: 38
ICS Code (Syringes, needles and catheters): 11.040.25

Document History

DIN EN ISO 11070
April 1, 2019
Sterile intravaskulaere Einfuehrungsinstrumente, Dilatatoren und Fuehrungsdraehte zur einmaligen Verwendung (ISO 11070:2014 + Amd 1:2018); Deutsche Fassung EN ISO 11070:2014 + A1:2018
A description is not available for this item.
DIN EN ISO 11070
October 1, 2018
Sterile single-use intravascular introducers, dilators and guidewires (ISO 11070:2014 + Amd 1:2018); German version EN ISO 11070:2014 + A1:2018
Diese Internationale Norm legt Anforderungen an Einführkanülen, Einführkatheter, Führungshülsen, Führungsdrähte und Dilatatoren fest, die steril geliefert werden und zur einmaligen Verwendung mit...
DIN EN ISO 11070/A1
January 1, 2018
Sterile single-use intravascular introducers, dilators and guidewires (ISO 11070:2014/DAM 1:2017); German and English version EN ISO 11070:2014/prA1:2017
A description is not available for this item.
DIN EN ISO 11070
March 1, 2015
Sterile single-use intravascular introducers, dilators and guidewires (ISO 11070:2014); German version EN ISO 11070:2014
Diese Internationale Norm legt Anforderungen an Einführkanülen, Einführkatheter, Führungshülsen, Führungsdrähte und Dilatatoren fest, die steril geliefert werden und zur einmaligen Verwendung mit...
DIN EN ISO 11070
July 1, 2013
Sterile, single-use intravascular introducers, dilators and guide wires (ISO/DIS 11070:2013); German version prEN ISO 11070:2013
A description is not available for this item.
DIN EN ISO 11070
July 1, 1999
Sterile single-use intravascular catheter introducers (ISO 11070:1998); German version EN ISO 11070:1999
A description is not available for this item.
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References

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 9626 - Stainless steel needle tubing for the manufacture of medical devices - Requirements and test methods
Published by ISO on August 1, 2016
This International Standard applies to rigid stainless steel needle tubing suitable for use in the manufacture of hypodermic needles and other medical devices primarily for human use. This...
This document references:
ISO 10555-3 - Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters
Published by ISO on June 15, 2013
This part of ISO 10555 specifies requirements for central venous catheters supplied in the sterile condition, and intended for single use.
This document references:
ISO 10555-5 - Intravascular catheters - Sterile and single-use catheters - Part 5: Over-needle peripheral catheters
Published by ISO on June 15, 2013
This part of ISO 10555 specifies requirements for over-needle peripheral intravascular catheters, intended for accessing the peripheral vascular system, supplied in the sterile condition and intended...
This document references:
ISO 10555-1 - Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements AMENDMENT 1
Published by ISO on November 1, 2017
A description is not available for this item.
This document references:
ISO 10555-4 - Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters
Published by ISO on June 15, 2013
This part of ISO 10555 specifies requirements for balloon dilatation catheters supplied in the sterile condition, and intended for single use.
This document references:
ISO 11135 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on July 15, 2014
Inclusions This International Standard specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the industrial...
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 7864 - Sterile hypodermic needles for single use - Requirements and test methods
Published by ISO on August 1, 2016
This International Standard specifies requirements for sterile hypodermic needles for single use of designated metric sizes 0,18 mm to 1,2 mm. It does not apply to those devices that are covered by...
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