Need help?

EN 27740:1992 Standard

wave
Save  

  Keywords:

#different #gradual #countries #manufacturers #transitional

This standard can be totally or partially supervised by:
  •   EN 27740:1992/A1:1997
  •   EN 27740:1992/AC:1996
  •   Directive

    Medical devices Directive (93/42/EEC)

      Last Official Journal reference

    Wednesday 14th of April 2021

      Description:

    Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)

      Purpose

    Lays down the dimensions of two sizes of fitting features for detacheable scalpel blades and the handles with which they are used. It secures a good fitting and interchangeability of detachable blades for scalpels manufactured in different countries or by different manufacturers. The transitional period for a gradual adaption of the fitting dimensions specified in this standard should end with the year 1990.

      Publication

    Friday 17th of November 2017

      Related Standards

    EN ISO 3826-2:2008

    Medical devices Directive (93/42/EEC)

    Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction...

    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 61676:2002/A1:2009

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiol...

    EN 62220-1-2:2007

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-2: Determination of the detective quantum...

    EN ISO 1135-4:2011

    Medical devices Directive (93/42/EEC)

    Transfusion equipment for medical use - Part 4: Transfusion sets for single use (ISO 1135-4:2010)

    EN 12342:1998+A1:2009

    Medical devices Directive (93/42/EEC)

    Breathing tubes intended for use with anaesthetic apparatus and ventilators

      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 27740:1992 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