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BS EN 45502-2-1-2003 Active implantable medical devices. Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)

Standard Number:  BS EN 45502-2-1-2003
Title:  Active implantable medical devices. Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
Language:  English
Replacing Standard:  BS 6902-1-1990, EN 50061-1988, BS 6902-1-Supplement No. 1-1996, EN 50061/A1-1995

Execute Date:  2004/1/20
Adopted International Standard:  EN 45502-2-1-2003
Status:  Current
CCS Classification for Standardschemical>>Synthetic materials>>Plastic material
Publisher:  British Standards
Price:  
Number of Pages:98  

Description:This Part 2-1 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES intended to treat bradyarrhythmias. The tests that are specified in EN 45502 are type tests, and are to be carried out on samples of a device to show compliance. This Part 2-1 is also applicable to some non-implantable parts and accessories of the devices (see Note 1). The characteristics of the IMPLANTABLE PULSE GENERATOR or LEAD shall be determined by either the appropriate method detailed in this Part 2-1 or by any other method demonstrated to have an accuracy equal to, or better than, the method specified. In the case of dispute, the method detailed in this Part 2-1 shall apply. Any features of an ACTIVE IMPLANTABLE MEDICAL DEVICE intended to treat tachyarrhythmias are covered by EN 45502-2-2. NOTE 1 The device that Is commonly referred to as an active implantable medical device may in fact be a single device, a combination of devices, or a combination of a device or devices and one or more accessories. Not all of these parts are required to be either partially or totally implantable, but there is a need to specify some requirements of non-implantable parts and accessories if they could affect the safety or performance of the implantable device. NOTE 2 The terminology used in this European Standard is intended to be consistent with the terminology of Directive 90/385/EEC. NOTE 3 In this European Standard, terms printed in small capital letters are used as defined in Clause 3. Where a defined term is used as a qualifier in another term, it is not printed in small capital letters unless the concept thus qualified is also defined.  
Cross References:EN 28601:1992; ISO 8601:1988; EN 45502-1:1997; EN 45502-2-2; EN 60068.2.27:1993; IEC 60068.2.27:1987; EN 60068.2.47:1999; IEC 60068-2-47:1999; EN 60068.2.64:1994; IEC 60068-2-64:1993; ISO 5841-3:1992; ISO 11318:1993; ANSI/AAMI PC69-2000; 90/385/EEC  
File Format:  PDF(Acrobat Reader) or Word version doc Document
File Size:  387KB
Tile in English:  Active implantable medical devices. Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)

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