PREN 45502-2-2 : DRAFT 1998

Foreword
Introduction
1 Scope
2 Normative references
3 Definitions
4 Symbols and abbreviations (optional)
5 General requirements for non-implantable parts
6 Measurement of implantable pulse generator and lead
   characteristics
7 General arrangement of the packaging
8 General markings for active implantable medical devices
9 Markings on the sales packaging
10 Construction of the sales packaging
11 Markings on the sterile pack
12 Construction of the non-reusable pack
13 Markings on the active implantable medical device
14 Protection from unintended biological effects being caused
   by the active implantable medical device
15 Protection from harm to the patient or user caused by
   external physical features of the active implantable medical
   device
16 Protection from harm to the patient caused by electricity
17 Protection from harm to the patient caused by heat
18 Protection from ionizing radiation released or emitted
   from the active implantable medical device
19 Protection from unintended effects caused by the device
20 Protection of the device from damage caused by external
   defibrillators
21 Protection of the device from changes caused by high
   power electrical fields applied directly to the patient
22 Protection of the active implantable medical device
   from changes caused by miscellaneous medical treatments
23 Protection of the active implantable medical device from
   mechanical forces
24 Protection of the active implantable medical device from
   damage caused by electrostatic discharge
25 Protection of the active implantable medical device from
   damage caused by atmospheric pressure changes
26 Protection of the active implantable medical device from
   changes caused by temperature changes
27 Protection of the active implantable medical device from
   electromagnetic non-ionizing radiation
28 Accompanying documentation
ANNEX AA (Informative) Table of cross-references from 90/385/EEC
                       and prEN 45502-1
ANNEX BB (Informative) Relationship between the clauses of this
                       standard and the essential requirements
                       (90/385/EEC) listed in Annex AA
ANNEX CC (Informative) Notes on EN 45502-3
ANNEX DD (Informative) Code for Describing Modes of the
                       implantable pulse generator
ANNEX EE (Informative) Interface Circuits
ANNEX FF (Informative) Selection of capacitor C[x]

Specifies requirements that are applicable to IMPLANTABLE CARDIOVERTER DEFIBRILLATORS and the functions of ACTIVE IMPLANTABLE MEDICAL DEVICES intended to treat tachyarrhythmia.