Back

EVS-EN 13726:2023

Test methods for wound dressings - Aspects of absorption, moisture vapour transmission, waterproofness and extensibility

General information

Valid from 02.10.2023
Base Documents
EN 13726:2023
ICS Groups
11.120.20 Wound dressings and compresses
Directives or regulations
None

Standard history

Status
Date
Type
Name
02.10.2023
Main
EVS-EN 13726:2023
01.06.2003
Main
EVS-EN 13726-3:2003
01.06.2003
Main
EVS-EN 13726-4:2003
01.09.2002
Main
EVS-EN 13726-1:2002
01.09.2002
Main
EVS-EN 13726-2:2002
This document specifies test methods for the evaluation of different performance characteristics of wound dressings, including absorbency, moisture vapour transmission rate, waterproofness and conformability.

Required fields are indicated with *

*
*
*
PDF
31.72 € incl tax
Paper
31.72 € incl tax
Browse standard from 2.44 € incl tax
Standard monitoring
English (PDF 491 KB)

Related products

Main

EVS-EN 13726-1:2002

Test methods for primary wound dressings - Part 1: Aspects of absorbency
Withdrawn from 02.10.2023
Main

EVS-EN 13726-4:2003

Non-active medical devices - Test methods for primary wound dressings - Part 4: Conformability
Withdrawn from 02.10.2023
Main

EVS-EN 13726-2:2002

Test methods for primary wound dressings - Part 2: Moisture vapour transmission rate of permeable film dressings
Withdrawn from 02.10.2023
Main

CEN/TR 15831:2009

Method for testing compression in medical hosiery
Newest version Valid from 04.06.2009

Customers who bought this item also bought

Main + amendment

EVS-EN ISO 11607-1:2020+A11+A1:2023

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2019 + ISO 11607-1:2019/Amd 1:2023)
Newest version Valid from 15.11.2023
Amendment

ISO 11607-2:2019/Amd 1:2023

Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1: Application of risk management
Newest version Valid from 13.09.2023
Amendment

EVS-EN ISO 11607-2:2020/A1:2023

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1 (ISO 11607-2:2019/Amd 1:2023)
Valid from 01.11.2023
Main

ISO 10993-17:2023

Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents
Newest version Valid from 13.09.2023

Standards designation

EVS Estonian standard
EN European standard (published by an CEN or CENELEC)
EN ISO International standard adopted as an European standard
ISO International Organization for Standardization’s standard
IEC International Electrotechnical Commission’s standard
HD CENELEC’s harmonisation document
   
EVS-EN European standard implemented in Estonia
EVS-EN ISO International standard adopted in Europe and implemented in Estonia
EVS-EN ISO/IEC International standard/International electrotechnical standard adopted in Europe and implemented in Estonia
EVS-IEC International electrotechnical standard implemented in Estonia
EVS-ISO International standard implemented in Estonia
   
A, AMD amedment
+A a full standard plus the amendment
/A only amendment
COR, AC corrigendum
+COR a full standard plus the corrigendum
NA national annex
+NA a full standard plus the national annex
/NA only national annex
TS technical specification
TR technical report
CWA agreement, developed by a CEN or CENELEC
prEVS-EN (etc) draft standard
   
et the standard is in Estonian only
en the standard is in English only
et-en the standard is in Parallel text Estonian-English