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About This Item

 

Full Description

BS EN ISO 10555-6:2017 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 ISO 10555 does not specify requirements, performance, and user safety issues related to non-coring needles.


Cross References:
EN ISO 10555-1 (ISO 10555-1:2013) AS
EN ISO 10555-3 (ISO 10555-3:2013) AS
ISO 10555-1:2013
ISO 10555-3:2013 ED2
ASTM F2119 - 07
ISO 17665-1:2006 Ed 1
ISO 48:2010
ISO 7864:2016
ISO 5832-2:1999
ISO 594-1:1986
ISO 5832-1:2016
ISO 10993-1:2009
ASTM F2052 - 06e1
ISO 11135-1:2007
ISO 9584:1993 (R08)
ISO 6474-1:2010 Ed 1
ASTM F2182 - 11a
ASTM F2213 - 06


All current amendments available at time of purchase are included with the purchase of this document.
 

Document History

  1. BS EN ISO 10555-6:2017+A1:2019


    Intravascular catheters. Sterile and single-use catheters-Subcutaneous implanted ports

    • Most Recent
  2. BS EN ISO 10555-6:2017

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    Intravascular catheters. Sterile and single-use catheters-Subcutaneous implanted ports

    • Historical Version
  3. BS ISO 10555-6:2015


    Intravascular catheters. Sterile and single-use catheters. Subcutaneous implanted ports

    • Historical Version