STN EN IEC 60601-2-33
| Name: | STN EN IEC 60601-2-33 |
| Validity: | Valid |
| Number of pages: | 152 |
| Language: |
EN
|
| Paper: | 36,30€ |
| Electronic version |
a) Only read (without ability to print and copy)
32,67€ b) Without ability to print, with ability to copy (printscreen) 36,30€ c) With ability to print and copy (printscreen) 47,19€ |
| Slovak title | Zdravotnícke elektrické prístroje. Časť 2-33: Osobitné požiadavky na základnú bezpečnosť a nevyhnutné prevádzkové vlastnosti prístrojov magnetickej rezonancie na zdravotnícku diagnostiku |
| English title | Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |
| Release Date: | 01. 01. 2025 |
| Date of withdrawal: | |
| ICS: | 11.040.55 |
| Sorting character/National clasification code | 36 4800 |
| Level of incorporation: | idt EN IEC 60601-2-33:2024, idt IEC 60601-2-33:2022 |
| Official Journal | 12/24 |
| Amendments | |
| Replaced by: | |
| Repleces: | STN EN 60601-2-33:2012-01 (36 4800) |
| Note in Official Journal: | |
| Subject of the standard: | This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MAGNETIC RESONANCE (MR) EQUIPMENT and MAGNETIC RESONANCE (MR) SYSTEMS. NOTE Where ME EQUIPMENT and ME SYSTEMS are used in the clause headings, this is to be understood to indicate MR EQUIPMENT and MR SYSTEMS. This document does not cover the application of MR EQUIPMENT beyond the INTENDED USE. If a clause or subclause is specifically intended to be applicable to MR EQUIPMENT only, or to MR 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 MR EQUIPMENT and to MR SYSTEMS, as relevant. This document does not formulate additional specific requirements for MR EQUIPMENT or MR SYSTEMS used in INTERVENTIONAL MR EXAMINATIONS. |
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