Medical Device Directive (MDD) in EU
GPTKB entity
Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
European Union law
|
| gptkbp:adoptedBy |
gptkb:European_Union
1993-06-14 |
| gptkbp:appliesTo |
gptkb:European_Economic_Area
|
| gptkbp:citation |
Directive 93/42/EEC
|
| gptkbp:enforcedBy |
national competent authorities
|
| gptkbp:enteredIntoForce |
1993-06-14
|
| gptkbp:establishesRequirementsFor |
gptkb:CE_marking
conformity assessment classification of medical devices essential requirements for safety and performance |
| https://www.w3.org/2000/01/rdf-schema#label |
Medical Device Directive (MDD) in EU
|
| gptkbp:legalStatus |
repealed
|
| gptkbp:officialName |
gptkb:Council_Directive_93/42/EEC
|
| gptkbp:purpose |
harmonize laws relating to medical devices in the EU
|
| gptkbp:relatedTo |
Active Implantable Medical Device Directive (AIMDD)
In Vitro Diagnostic Medical Devices Directive (IVDD) |
| gptkbp:repealedBy |
2021-05-26
Medical Device Regulation (MDR) (EU) 2017/745 |
| gptkbp:replacedBy |
Medical Device Regulation (MDR) (EU) 2017/745
|
| gptkbp:subject |
medical devices
|
| gptkbp:bfsParent |
gptkb:Medical_Device_Regulation
|
| gptkbp:bfsLayer |
7
|