GE OEC Medical Systems
GE OEC Medical Systems
Address(es) |
|
Website | Not available |
Status | MEMBER |
Acceptance date | 2023-04-13 |
Further information
Stage | Country | Name |
---|---|---|
2 | Canada |
LEGEND: Scope Limitations
- RA : Audio amplifiers with audio power > 0,5 Watts excluded
- RC : Apparatus with connection(s) to a cable distribution system excluded
- RSH : Shredders excluded
- RT : Apparatus with connection(s) to a telecommunication network excluded
- RV : CRT (cathode ray tubes)/ picture tubes, plasma/LCD or other video apparatus excluded
- ROUT : Equipment intended for installation outdoors excluded
- RWPT : Wireless power transmitter excluded
Category | Name | Tests/Clauses | Acceptance Date | Responsible National Certification Body |
---|---|---|---|---|
MED | IEC 60601-1:2005 | All clauses except 36 (EMC) and 48 (Biocompatibility) | 2016-07-14 | |
MED | IEC 60601-1:2005/AMD1:2012 | All clauses except 36 (EMC) and 48 (Biocompatibility) | 2016-07-14 | |
MED | IEC 60601-1:2005/AMD2:2020 | Medical Electrical Equipment - Part 1: General Requirements for basic safety and essential performanceAll except: Biocompatibility (Cl. 11.7) and EMI/EMC (Cl. 17) | 2022-03-30 | |
MED | IEC 60601-1-3:2008 | All Clauses | 2016-07-14 | |
MED | IEC 60601-1-3:2008/AMD1:2013 | All clauses | 2019-09-24 | |
MED | IEC 60601-1-3:2008/AMD2:2021 | Medical Electrical Equipment - Part 1-3: General requirements for basic safety and essential performance. Collateral standard: Radiation Protection in Diagnostic x-ray Equipment | 2022-03-30 | |
MED | IEC 60601-1-6:2010 | All Clauses | 2016-07-14 | |
MED | IEC 60601-1-6:2010/AMD1:2013 | All Clauses | 2016-07-14 | |
MED | IEC 60601-1-6:2010/AMD2:2020 | Medical Electrical Equipment - Part 1-6: General requirements or basic saety and essential performance - Collateral Standards: Usability | 2022-03-30 | |
MED | IEC 60601-1-8:2006/AMD2:2020 | All clauses | 2022-03-30 | |
MED | IEC 60601-2-28:2017 | All clauses | 2019-09-24 | |
MED | IEC 60601-2-28:2010 | All Clauses | 2016-07-14 | |
MED | IEC 60601-2-43:2022 | All | 2024-04-22 | |
MED | IEC 60601-2-43:2010 | All Clauses | 2016-07-14 | |
MED | IEC 60601-2-43:2010/AMD1:2017 | All clauses | 2018-12-06 | |
MED | IEC 60601-2-43:2010/AMD2:2019 | Medical Electrical Equipment - Part 2-43: Particular Requirements for the safety and essential performance of X-ray equipment for interventional procedures | 2022-03-30 | |
MED | IEC 60601-2-54:2022 | All | 2024-04-22 | |
MED | IEC 60601-2-54:2009 | All Clauses | 2016-07-14 | |
MED | IEC 60601-2-54:2009/AMD1:2015 | All clauses | 2018-12-06 | |
MED | IEC 60601-2-54:2009/AMD2:2018 | All clauses | 2020-03-16 |