iTeh StandardsiTeh Standards
EURUSD
Your shopping cart is empty.
SIST

SIST EN 27740:2000

(Main)

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

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

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.

Chirurgische Instrumente, Skalpelle mit auswechselbaren Klingen, Paßmaße (ISO 7740:1985)

Instruments chirurgicaux, bistouris a lames détachables, dimensions d'assemblage (ISO 7740:1985)

La présente Norme internationale fixe les dimensions de deux types d'assemblages de lames détachables et de manches de bistouris correspondants.

Kirurški instrumenti, skalpeli s snemnimi rezili, mere nastavkov (ISO 7740:1985)

General Information

Status
Published
Publication Date
31-Dec-1999
ICS
11.040.30 - Surgical instruments and materials
Technical Committee
VAZ - Healthcare
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
01-Jan-2000
Due Date
01-Jan-2000
Completion Date
01-Jan-2000
Directive
93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Mandate
M/023 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
Ref Project
EN 27740:1992 - Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)

Relations

Amended By
SIST EN 27740:2000/A1:2000 - Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)
Effective Date
22-Dec-2008
Corrected By
SIST EN 27740:2000/AC:2000 - Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)
Effective Date
22-Dec-2008

Buy Standard

EN 27740:2000EN 27740:2000
PreviousNext
Standard
EN 27740:2000
English language
5 pages
sale 10% off
Preview
sale 10% off
Preview
e-Library read for
1 day

Standards Content (Sample)


SLOVENSKI STANDARD
01-januar-2000
Kirurški instrumenti, skalpeli s snemnimi rezili, mere nastavkov (ISO 7740:1985)
Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO
7740:1985)
Chirurgische Instrumente, Skalpelle mit auswechselbaren Klingen, Paßmaße (ISO
7740:1985)
Instruments chirurgicaux, bistouris a lames détachabl
...

Questions, Comments and Discussion

Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.

This May Also Interest You

SIST
SIST EN ISO 13402:2025(Main)
Surgical and dental hand instruments - Determination of resistance against autoclaving, corrosion and thermal exposure (ISO 13402:2025)
EN ISO 13402:2025

This document describes test methods to determine the resistance of stainless steel surgical and dental hand instruments against autoclaving, corrosion and thermal exposure.

  • Standard
    26 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN ISO 16061:2021(Main)
Instruments for use in association with non-active surgical implants - General requirements (ISO 16061:2021)
EN ISO 16061:2021

This document specifies the general requirements for instruments to be used in association with non-active surgical implants. These requirements apply to instruments when they are manufactured and when they are supplied after refurbishment.
NOTE     In this document, unless otherwise specified, the term "instrument" refers to an instrument for use in association with non-active surgical implants.
This document also applies to instruments which can be connected to power-driven systems, but it does not apply to the power-driven systems themselves.
With regard to safety, this document gives the requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging, and information supplied by the instrument manufacturer, hereafter referred to as the manufacturer.
This document is not applicable to instruments associated with dental implants, transendodontic and transradicular implants and ophthalmic implants.

  • Standard
    23 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN ISO 7153-1:2017(Main)
Surgical instruments - Materials - Part 1: Metals (ISO 7153-1:2016)
EN ISO 7153-1:2016

ISO 7153-1:2016 specifies metals commonly used to manufacture various types of standard surgical instruments, including but not limited to those used in general surgery, orthopaedics and dentistry.
While ISO 7153-1:2016 is not intended for surgical instruments used in special applications, such as implantology and minimally invasive surgery, parts of it might be applicable to those instruments.

  • Standard
    20 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN ISO 11810:2016(Main)
Lasers and laser-related equipment - Test method and classification for the laser resistance of surgical drapes and/or patient protective covers - Primary ignition, penetration, flame spread and secondary ignition (ISO 11810:2015)
EN ISO 11810:2015

ISO 11810:2015 is applicable to disposable and reusable, as well as woven and non-woven materials used as surgical drapes and other patient-protective covers which claim to be laser-resistant. The purpose of this International Standard is to provide a standardized method for testing and classifying surgical drapes and other patient-protective covers with respect to laser-induced hazards. An appropriate classification system is given. It is not the purpose of this International Standard to serve as a general fire safety specification, and as such, this International Standard does not cover other sources of ignition.
All materials reflect portions of the beam and it is necessary for the user to decide whether specular reflectance can be a hazard. This measurement, however, is not covered in this International Standard.
The test procedure can be used to assess the laser induced flammability properties of non-laser-resistant items
NOTE          Users of products tested by this method are cautioned that the laser resistance of a surgical drape and/or patient-protective cover will be wavelength sensitive and that a surgical drape and/or patient-protective cover are better tested at the wavelength for which it is intended to be used. If tested using other wavelengths, it is necessary to explicitly state the power settings and modes of delivery.

  • Standard
    29 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 27740:2000/A1:2000(Amendment)
Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)
EN 27740:1992/A1:1997

2020-01-20: Originator of XML version: NEN (on behalf of NEN, ASI, DS, SFS, SIS, SN)

  • Amendment
    4 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 27740:2000/AC:2000(Amendment)
Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)
EN 27740:1992/AC:1996
  • Corrigendum
    4 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN ISO 13402:2025(Main)
Surgical and dental hand instruments - Determination of resistance against autoclaving, corrosion and thermal exposure (ISO 13402:2025)
EN ISO 13402:2025

This document describes test methods to determine the resistance of stainless steel surgical and dental hand instruments against autoclaving, corrosion and thermal exposure.

  • Standard
    26 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN IEC 60601-2-2:2018/A1:2024(Amendment)
Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories (IEC 60601-2-2:2017/AMD1:2023)
EN IEC 60601-2-2:2018/A1:2024

No scope available

  • Amendment
    13 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN IEC 80601-2-77:2021/A1:2024(Amendment)
Medical electrical equipment - Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment (IEC 80601-2-77:2019/AMD1:2023)
EN IEC 80601-2-77:2021/A1:2023
  • Amendment
    11 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN IEC 60601-2-41:2022(Main)
Medical electrical equipment - Part 2-41: Particular requirements for the basic safety and essential performance of surgical luminaires and luminaires for diagnosis (IEC 60601-2-41:2021)
EN IEC 60601-2-41:2021

IEC 60601-2-41:2021 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of SURGICAL LUMINAIRES and LUMINAIRES FOR DIAGNOSIS, hereafter referred to as ME EQUIPMENT.
If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.
This particular standard does not apply to
– headlights;
– endoscopes, laparoscopes and their light sources, which are covered by IEC 60601-2-18;
– luminaires used in dentistry, which are covered by ISO 9680;
– luminaires for general purposes, which are covered by IEC 60598-2-1 and IEC 60598-2-4;
– luminaires dedicated to therapeutic purposes;
– special purpose lights with different conditions of use such as light sources intended solely for decontamination of air and surfaces, UV lights for dermatological diagnosis, slit lamps for ophthalmology, lights for surgical microscopes and lights for surgical navigation systems;
– lights connected to surgical instruments, such as luminous retractors;
– luminaires for emergency lighting, which are covered by IEC 60598-2-22.
SURGICAL LUMINAIRES and LUMINAIRES FOR DIAGNOSIS are medical devices and not general lighting equipment.
IEC 60601-2-41:2021 cancels and replaces the second edition published in 2009 and Amendment 1:2013. This edition constitutes a technical revision.
This edition includes the following significant technical changes with respect to the previous edition:
a) revised the statement of essential performance;
b) added exposure limits, test conditions, calculation methods and safety warnings related to photobiological hazards;
c) removed the terms “MINOR SURGICAL LUMINAIRES” and “MAJOR SURGICAL LUMINAIRES”;
d) added definitions of MAXIMUM ILLUMINANCE DISTANCE and REFERENCE DISTANCE and allowed MANUFACTURERS to measure some performance characteristics at the REFERENCE DISTANCE that they specify;
e) replaced the region of acceptable chromaticity in (x,y) colour space with a requirement for Du,v;
f) added a requirement for acceptable drift of the lighthead when attached to the suspension system;
g) added a requirement for fluid ingress protection;
h) revised Table 201.101 of IEC 60601-2-41:2009 and IEC 60601-2-41:2009/AMD1:2013 and moved it to Annex BB;
i) specified a new device for measuring SHADOW DILUTION in a simulated cavity;
j) specified test conditions for luminaires equipped with distance sensors.

  • Standard
    63 pages
    English language
    sale 10% off
    e-Library read for
    1 day