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EN 60601-2-28:1993

(Main)

Medical electrical equipment - Part 2: Particular requirements for the safety of X-ray source assemblies and X-ray tube assemblies for medical diagnosis

Medical electrical equipment - Part 2: Particular requirements for the safety of X-ray source assemblies and X-ray tube assemblies for medical diagnosis

Specifies the safety requirements for X-ray tube assemblies for medical diagnoses and components thereof, specified for use in medical X-ray equipment including equipment for computed tomography, that incorporates a specified high-voltage generator complying with HD 395.2.7 or HD 395.2.15.

Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von Röntgenstrahler einschließlich Blendensystem für medizinische Diagnostik

Appareils éléctromédicaux - Partie 2: Règles particulières de sécurité pour les ensembles radiogènes à rayonnement X et les gaines équipées pour diagnostic médical

Spécifie les prescriptions de sécurité pour les ensembles radiogènes à rayonnement X et les gaines équipées pour diagnostic médical et aux composants de ceux-ci, spécifiés pour utilisations dans un équipement à rayonnement X, y compris les équipements pour tomodensitométrie, qui comprennent un générateur radiologique spécifié en conformité avec HD 395.2.7 ou la HD 395.2.15

Medicinska električna oprema - 2. del: Posebne varnostne zahteve za vire rentgenskih žarkov in sklope rentgenskih cevi za medicinsko diagnostiko (IEC 60601-2-28:1993)

General Information

Status
Withdrawn
Publication Date
27-May-1993
Withdrawal Date
28-Feb-1994
Technical Committee
CLC/TC 62 - Electrical equipment in medical practice
Drafting Committee
IEC/SC 62B - IEC_SC_62B
Parallel Committee
IEC/SC 62B - IEC_SC_62B
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
01-Apr-2013
Completion Date
01-Apr-2013
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
M/432 - Standardisation Mandate addressed to CEN and CENELEC within the framework of Directive 2007/47/EC amending Directive 90/385/EEC and Directive 93/42/EEC relating to Medical Devices
Ref Project
SIST EN 60601-2-28:1995 - Medical electrical equipment - Part 2: Particular requirements for the safety of X-ray source assemblies and X-ray tube assemblies for medical diagnosis

Relations

Replaced By
EN 60601-2-28:2010 - Medical electrical equipment - Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis
Effective Date
28-Jan-2023
Replaced By
EN 60601-2-54:2009 - Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy
Effective Date
28-Jan-2023

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EN 60601-2-28:1995EN 60601-2-28:1995
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EN 60601-2-28:1995
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Standards Content (Sample)


SLOVENSKI STANDARD
01-maj-1995
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UHQWJHQVNLKåDUNRYLQVNORSHUHQWJHQVNLKFHYL]DPHGLFLQVNRGLDJQRVWLNR ,(&

Medical electrical equipment - Part 2: Particular requirements for the safety of X-ray
source assemblies and X-ray tube assemblies for medical diagnosis
Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von
Röntgenstrahler einschließlich Blendensystem für medizinische Diagnostik
Appareils éléctromédicaux - Partie 2: Règles particulières de sécurité pour les
ensembles radiogènes à rayonnement X et les gaines équipées pour diagnostic médical
Ta slovenski standard je istoveten z: EN 60601-2-28:1993
ICS:
11.040.50 Radiografska oprema Radiographic equipment
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

SIST
...

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