CENELEC - Standards Development - List of Technical Bodies - CEN/CLC/JWG AIMD
Button back to homepage

CENELEC
International Standards and Conformity Assessment for all electrical, electronic and related technologies

CEN/CLC/JWG AIMD

CEN/CENELEC Joint Working Group Active Implantable Medical Devices
 
 
export to xls file

CEN/CLC/JWG AIMD Work programme

sort up 
Project reference
sort upsort down
Current Code
sort upsort down
Document
Init. Date
sort upsort down
Current stage
sort upsort down
Next Stage
sort upsort down
Fcst. voting date
prEN 45502-1:2013 (pr=22891)
Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer
4020 2010-03-222013-04-262013-07-262012-04-30

export to xls file

CEN/CLC/JWG AIMD Publications

Reference, Title
sort up  
Publication date
sort up sort down
Downloads
EN 45502-1:1997 (pr=4943)
Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer		1997-08-27 export to doc file  EN
EN 45502-2-1:2003 (pr=7407)
Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)		2003-12-22 export to doc file  EN
EN 45502-2-2:2008 (pr=8622)
Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)		2008-03-31 export to doc file  EN  FR  DE
EN 45502-2-3:2010 (pr=12942)
Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems		2010-02-19 export to doc file  EN  FR  DE

export to xls fileexport to xls file

CEN/CLC/JWG AIMD Maintenance cycle

 sort down
Publication number
sort upsort down
Date of Publication
Review date
sort upsort down
Result date
sort upsort down
Technical Comittee
sort upsort down
Project in progress
EN 45502-1:1997 (pr=4943)
Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer		1997-08-272010-05-012013-05-01CEN/CLC/JWG AIMDprEN 45502-1:2013
EN 45502-2-1:2003 (pr=7407)
Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)		2003-12-222008-12-222011-12-22CEN/CLC/JWG AIMD 
EN 45502-2-2:2008 (pr=8622)
Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)		2008-03-312013-03-312016-03-31CEN/CLC/JWG AIMD 
EN 45502-2-3:2010 (pr=12942)
Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems		2010-02-192015-02-192018-02-19CEN/CLC/JWG AIMD 

export to xls file

TC 3 Project files


CEN/CLC/JWG AIMD TC/SC in figures

Current Stage
Year
Year -1
Year -2
Year -3
Year -4
Year >5
Enquiry stage100000
Published000103

CEN/CLC/JWG AIMD Figures overall

Total publications
 32
Published in last 3 years
 7
Total work in progress
 15
Total proposals
 0
export to xls file

CEN/CLC/JWG AIMD Environment

Reference
Clause
Categories - Aspects
Product Life Cycle
Information
Confirmed

export to xls file

CEN/CLC/JWG AIMD EU Directive(s)

Reference
Stage code
Directive
OJ Status
OJ Reference
Mandate
EN 45502-1:1997 (pr=4943)
Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer		 6060 90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices		 PUB C 22/01 M/432
prEN 45502-1:2013 (pr=22891)
Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer		 4020 90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices		 NEW M/432
EN 45502-2-1:2003 (pr=7407)
Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)		 6060 90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices		 PUB C 22/01 M/432
EN 45502-2-2:2008 (pr=8622)
Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)		 6060 90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices		 PUB C 22/01 M/432
EN 45502-2-3:2010 (pr=12942)
Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems		 6060 90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices		 PUB C 22/01 M/432

 
Share facebook linkedIn linkedIn
Privacy | Contact
Copyright © CENELEC . All rights reserved.