Statements (14)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:International_Standard
|
| gptkbp:appliesTo |
in vitro diagnostic medical equipment
|
| gptkbp:firstPublished |
2002
|
| gptkbp:language |
gptkb:French
English |
| gptkbp:latestReleaseVersion |
2018
|
| gptkbp:partOf |
gptkb:IEC_61010_series
|
| gptkbp:publishedBy |
gptkb:International_Electrotechnical_Commission
|
| gptkbp:scope |
Safety requirements for IVD medical equipment
|
| gptkbp:standardNumber |
gptkb:IEC_61010-2-101
|
| gptkbp:title |
gptkb:Safety_requirements_for_electrical_equipment_for_measurement,_control,_and_laboratory_use_–_Part_2-101:_Particular_requirements_for_in_vitro_diagnostic_(IVD)_medical_equipment
|
| gptkbp:bfsParent |
gptkb:IEC_61010
|
| gptkbp:bfsLayer |
6
|
| https://www.w3.org/2000/01/rdf-schema#label |
IEC 61010-2-101
|