Publication details
| Publication CODE |
Title |
| NBN EN IEC 80601-2-26:2020 (2020-04) |
MEDICAL ELECTRICAL EQUIPMENT - PART 2-26: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROENCEPHALOGRAPHS |
| |
| Price Excl. VAT |
Total number of pages, tables and drawings |
|
25.00 €
|
4. |
Description
IEC 80601-2-26:2019 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTROENCEPHALOGRAPHS as defined in 201.3.204, hereafter also referred to as ME EQUIPMENT or ME SYSTEM. This document is applicable to ELECTROENCEPHALOGRAPHS intended for use in professional healthcare facilities, the EMERGENCY MEDICAL SERVICES ENVIRONMENT or the HOME HEALTHCARE ENVIRONMENT.
This document does not cover requirements for other equipment used in electroencephalography such as:
- phono-photic stimulators;
- EEG data storage and retrieval;
- ME EQUIPMENT particularly intended for monitoring during electro-convulsive therapy.
If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title or 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 follows.
The clause or subclause applies to ME EQUIPMENT, as default. For ME EQUIPMENT with the corresponding safety measure or function not completely integrated into the ME EQUIPMENT but instead implemented in an ME SYSTEM, the ME EQUIPMENT MANUFACTURER specifies in the ACCOMPANYING DOCUMENTS which functionality and safety requirements are provided by the ME SYSTEM to comply with this document. The ME SYSTEM is verified accordingly.
HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this document are not covered by specific requirements in this document.
IEC 80601-2-26:2019 cancels and replaces the third edition of IEC 60601-2-26 published in 2012. This edition constitutes a technical revision to align with Amendment 1:2012 of IEC 60601-1:2005, new versions of collateral standards and amendments thereto.
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| Class |
C
|
Available files
ATTENTION: Belgian registered standards (NBN EN or NBN HD) are generally
only available in English or French. Only the cover page is translated
and the document itself is in English or in French.
Very important notice: 98% of the text of the NBN EN 55XXX,
NBN EN 6XXXX comes from the IEC text which is NOT included.
This text can be ordered here:
IEC 80601-2-26:2019.
For the series NBN EN 50XXX, the standards are however complete.
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DE version
|
EN version
|
FR version
|
|
Status
| Status |
Registered trilingual Belgian standard EN or FR or DE |
| Situation |
Currently active
Replaces
NBN EN 60601-2-26:2015
|
|
Origin
| Committee |
CLC/TC 62
Electrical equipment in medical practice
|
Approval
| BEC Approval |
2020-01-01 |
| NBN Approval |
2020-04-29 |
| Numbers identifying the european directives |
93/42/EEC
(Medical devices)
|
| ICS-Code (International Standards Classification) |
11.040.55
, 11.040.99
|
| NBN Status |
New |
|
| Date of ratification (d.o.r.) |
2020-01-01 |
| Date of availability (d.a.v.) |
2020-04-03 |
| Date of announcement (d.o.a.) |
2020-07-03 |
| Date of publication (d.o.p.) |
2020-10-03 |
| Date of withdrawal former edition (d.o.w.) |
2023-04-03 |
|
Correspondences with international standards
| Relation |
International standard |
Date |
| is identical to |
EN IEC 80601-2-26:2020
|
2020-04-03 |
| is identical to |
IEC 80601-2-26:2019
|
2019-05-20 |
Relations to belgian/foreign publications
| Type |
Origin |
Code |
Date |
| Standard |
Foreign |
IEC 60601-1-12:2014 |
|
| Standard |
Belgium |
NBN EN 60601-1-11:2015 |
|
| Standard |
Belgium |
NBN EN 60601-1-2:2015 |
|
| Standard |
Belgium |
NBN EN 60601-1-6:2010/A1:2015 |
|
| Standard |
Belgium |
NBN EN 60601-1:2007 |
|
| Standard |
Belgium |
NBN EN IEC 60601-2-2:2018 |
|
|
