Norm

NEN-EN-IEC 60601-2-68:2015 en

Medische elektrische toestellen - Deel 2-68: Bijzondere eisen voor basisveiligheid en essentiële prestaties van op röntgenstraling gebaseerde beeldgeleide radiotherapietoestellen voor gebruik met elektronenversnellers, lichte ionenbundel therapietoestellen en radionucleïdebundel therapietoestellen

253,59

Over deze norm

Status Definitief
Aantal pagina's 130
Commissie Medische elektrische toestellen
Gepubliceerd op 01-06-2015
Taal Engels
NEN-EN-IEC 60601-2-68 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of X-ray based IMAGE-GUIDED RADIOTHERAPY equipment for use with EXTERNAL BEAM EQUIPMENT (EBE). This particular standard covers safety aspects of kilovoltage (kV) and megavoltage (MV) X-ray imaging devices in a known geometrical relationship with EBE for the purpose of IGRT. It covers aspects of communication and relationships between the EXTERNAL BEAM EQUIPMENT and X-ray imaging devices, attached or not directly attached to, but in the same RADIATION shielded area as, and dedicated for use only with, the EXTERNAL BEAM EQUIPMENT. This particular standard deals with equipment for REAL-TIME X-IGRT, ONLINE X-IGRT and OFFLINE X-IGRT. It covers procedures to reduce the risk of over-reliance on the X-IGRT EXTERNAL BEAM SYSTEM (X-IGRT EBS). For example the manufacturer will provide an interactive interface for user interaction with the correction suggested by the system. If a clause or subclause is specifically intended to be applicable to X-IGRT EBE SYSTEMS the content of that clause or subclause will say so. If that is not the case, the clause or subclause applies only to X-IGRT EQUIPMENT. This particular standard, with the inclusion of TYPE TESTS and SITE TESTS, applies respectively to the MANUFACTURER and some installation aspects of X-IGRT EBE SYSTEMS intended to be • for NORMAL USE, operated under the authority of appropriately licensed or QUALIFIED PERSONS by OPERATORS having the required skills for a particular medical application, for particular specified clinical purposes, e.g. STATIONARY RADIOTHERAPY or MOVING BEAM RADIOTHERAPY, • maintained in accordance with the recommendations given in the INSTRUCTIONS FOR USE, • subject to regular quality assurance performance and calibration checks by a QUALIFIED PERSON.

Details

ICS-code 11.040.60
Nederlandse titel Medische elektrische toestellen - Deel 2-68: Bijzondere eisen voor basisveiligheid en essentiële prestaties van op röntgenstraling gebaseerde beeldgeleide radiotherapietoestellen voor gebruik met elektronenversnellers, lichte ionenbundel therapietoestellen en radionucleïdebundel therapietoestellen
Engelse titel Medical electrical equipment - Part 2-68: Particular requirements for the basic safety and essential performance of X-ray-based image-guided radiotherapy equipment for use with electron accelerators, light ion beam therapy equipment and radionuclide beam therapy equipment
Normatieve verwijzingen
  • 93/42/EEG, Medische hulpmiddelen

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