ISO 20697:2018
Current
The latest, up-to-date edition.
Sterile drainage catheters and accessory devices for single use
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
French, English
05-06-2018
This document specifies requirements for sterile, single use drainage catheters, wound and fluid accumulation drainage systems, surgical drainage catheters and their components, where the catheter is placed in a body cavity or wound, surgically or percutaneously, for drainage of fluid or air to the exterior.
The drainage catheter is left to drain naturally or connected to a suction source for faster tissue granulation.
This document is not applicable to:
a) suction catheters;
b) tracheal catheters;
c) urethral catheters;
NOTE See ISO 20696.
d) ureteral stents, biliary stents, and other stents;
NOTE See ISO 14630 and ASTM F1828‑97 for stents requirements.
e) drainage catheters placed in digestive tracts percutaneously with gastrostomy technique;
f) neuraxial catheters used for removal of cerebrospinal fluid;
NOTE See ISO 20698.
g) enteral catheters used for removal of solutions or substances from the gastrointestinal tract;
NOTE See ISO 20695.
h) coatings.
Committee |
ISO/TC 84
|
DevelopmentNote |
Supersedes ISO/DIS 20697. (06/2018)
|
DocumentType |
Standard
|
Pages |
38
|
ProductNote |
THIS STANDARD ALSO REFERS TO ISO 20695 THIS STANDARD HAVE CORRECTED VERSION FOR ENGLISH AND FRENCH 2018
|
PublisherName |
International Organization for Standardization
|
Status |
Current
|
Standards | Relationship |
UNE-EN ISO 20697:2019 | Identical |
SN EN ISO 20697 : 2019 | Identical |
NF EN ISO 20697 : 2018 | Identical |
DIN EN ISO 20697:2019-04 | Identical |
I.S. EN ISO 20697:2018 | Identical |
SS-EN ISO 20697 : 2018 | Identical |
EN ISO 20697:2018 | Identical |
ÖNORM EN ISO 20697: 2019 02 01 | Identical |
I.S. EN ISO 20697:2018&LC:2018 | Identical |
IS 18451 : 2023 | Identical |
BS EN ISO 20697:2018 | Identical |
DIN 13273-7:2003-08 | CATHETER FOR MEDICAL USE - PART 7: DETERMINATION OF THE X-RAY ATTENUATION OF CATHETERS - REQUIREMENTS AND TESTING |
ISO 11135:2014 | Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices |
ASTM F 1842 : 2015 : REDLINE | Standard Test Method for Determining Ink or Coating Adhesion on Flexible Substrates for a Membrane Switch or Printed Electronic Device |
ISO/TR 19244:2014 | Guidance on transition periods for standards developed by ISO/TC 84 — Devices for administration of medicinal products and catheters |
ISO 14630:2012 | Non-active surgical implants — General requirements |
EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
ASTM F 2052 : 2015 : REDLINE | Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment |
ASTM F 2213 : 2017 : REDLINE | Standard Test Method for Measurement of Magnetically Induced Torque on Medical Devices in the Magnetic Resonance Environment |
ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 80369-1:2010 | Small-bore connectors for liquids and gases in healthcare applications Part 1: General requirements |
ISO 14155:2011 | Clinical investigation of medical devices for human subjects Good clinical practice |
ASTM F 1828 : 2017 : REDLINE | Standard Specification for Ureteral Stents |
ISO 14971:2007 | Medical devices Application of risk management to medical devices |
ISO 15223-1:2016 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
EN 980:2008 | Symbols for use in the labelling of medical devices |
ASTM F 640 : 2012 : REDLINE | Standard Test Methods for Determining Radiopacity for Medical Use |
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