CEI EN 60580 PDF

CEI EN 60580 PDF

Name:
CEI EN 60580 PDF

Published Date:
08/01/2001

Status:
[ Revised ]

Description:

Medical electrical equipment - Dose area product meters

Publisher:
Comitato Elettrotecnico Italiano

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

SKU:

Choose Document Language:
$16.8
Need Help?
BLINGUAL * W/D S/S BY CEI EN IEC 60580

La norma si riferisce alle prestazioni e alle prove dei sistemi di misura del prodotto dose-area con camere a ionizzazione previste per la misura del prodotto dose-area al quale il paziente è esposto durante gli esami radiologici.
Include le prescrizioni per una prestazione soddisfacente dell’apparecchiatura come pure uniforma i metodi per determinare la conformità alla prestazione prevista.
La presente Norma annulla e sostituisce la CEI 62-7:1998, la quale tuttavia rimane in vigore in parallelo fino al 01-02-2003.


Edition : 2
File Size : 1 file , 410 KB
Number of Pages : 42
Published : 08/01/2001

History

CEI EN IEC 60580
Published Date: 09/01/2020
Medical electrical equipment - Dose area product meters
$23.1
CEI EN 60580
Published Date: 08/01/2001
Medical electrical equipment - Dose area product meters
$16.8

Related products

CEI EN IEC 61280-1-4
Published Date: 06/01/2023
Fibre optic communication subsystem test procedures Part 1-4: General communication subsystems - Light source encircled flux measurement method
$20.1
CEI UNI EN ISO/IEC 17000
Published Date: 02/01/2021
Conformity assessment - Vocabulary and general principles
$21.3
CEI EN IEC 60076-11
Published Date: 07/01/2019
Power transformers Part 11: Dry-type transformers
$39.3
CEI EN IEC 61169-1-4
Published Date: 04/01/2021
Radio-frequency connectors Part 1-4: Electrical test methods - Voltage standing wave ratio, return loss and reflection coefficient
$13.5

Best-Selling Products

MEDDEV 13/93
Published Date:
Guidelines Relating to the Application of: The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices
MEDDEV 2.1/3
Published Date: 03/01/1998
Guidelines Relating to the Demarcation Between 90/385/EEC on Active Implatable Medical Devices, 93/42/EEC on Medical Devices,65/65/EEC Relating to Medicinal Products & Related Directives
MEDDEV 3/94
Published Date: 04/01/1994
Guidelines Relating to the Application of : The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices