Need help?

EN 13718-1:2008 Standard

wave
Save  

  Keywords:

#conditions #standard #requirements #european #ambulances

  This standard is no longer addressed in the last official Journal publication of the "2021-04-14 ". This standard is addressed for the last time in the official journal publication of the "2020-03-25"

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 25th of March 2020

  Description:

Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances

  Purpose

This European Standard specifies general requirements for medical devices carried in air ambulances and used therein and outside hospitals and clinics in situations where the ambient conditions can differ from normal indoor conditions. This European Standard does not cover the requirements for approval and registration of the vehicle and the training of the staff which is the responsibility of the authority/authorities in the country where the ambulance is to be registered.

  Publication

Friday 17th of November 2017

  Cessation

This standard has been withdrawn on 2021-04-14

  Reference

This standard supersedes the "EN 13718-1:2002"

Anyway is still possible use the "EN 13718-1:2002" until February 28th, 2009

  Related Standards

EN ISO 13485:2016/AC:2016

Medical devices Directive (93/42/EEC)

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)

EN ISO 25424:2019

Medical devices Directive (93/42/EEC)

Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and rout...

EN ISO 22442-2:2020

Medical devices Directive (93/42/EEC)

Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-...

EN ISO 22442-1:2020

Medical devices Directive (93/42/EEC)

Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2020)

EN ISO 14607:2018

Medical devices Directive (93/42/EEC)

Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2018, Corrected version 2018-08)

EN ISO 14155:2020

Medical devices Directive (93/42/EEC)

Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)

  Stay up to date

CELAB is Notified Body No.2037 for the EMC Directive and Italian office of a Notified Body for the RED Directive.

CELAB performs voluntary inspection activities on technical construction files to check their contents.

CELAB can accomplish all the required tests in order to affix the CE-marking related to EMC, LVD, RED, MDD, machines and many others.

CLICK HERE TO GET TESTS AND INFO ON THE EN 13718-1:2008 STANDARD

  ACCESS

Search for a standard
GO

Register

Already a member?
Login

  OTHER APPLICATIONS

If you are interested in DO160 tests, you can give a try to our other free of charge software:
CE-Marking assistant, Version: 1.3.0