Statements (65)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:standard
|
| gptkbp:bfsLayer |
7
|
| gptkbp:bfsParent |
gptkb:IEC_60601_series
|
| gptkbp:addresses |
electromagnetic interference
|
| gptkbp:aims_to |
safety and performance of medical devices
|
| gptkbp:amended_by |
gptkb:2014
|
| gptkbp:applies_to |
gptkb:hospital
medical electrical equipment surgical devices |
| gptkbp:collaborated_with |
industry partners
international experts |
| gptkbp:developed_by |
technical committees
|
| gptkbp:first_published |
gptkb:2007
|
| gptkbp:focuses_on |
electromagnetic compatibility
|
| https://www.w3.org/2000/01/rdf-schema#label |
IEC 60601-1-2
|
| gptkbp:includes_provisions_for |
emission and immunity testing
|
| gptkbp:is_adopted_by |
many countries
telemedicine applications |
| gptkbp:is_aligned_with |
global standards
|
| gptkbp:is_associated_with |
patient monitoring equipment
|
| gptkbp:is_challenged_by |
emerging technologies
new regulations |
| gptkbp:is_cited_in |
medical device approvals
|
| gptkbp:is_considered |
product development
risk assessment processes |
| gptkbp:is_critical_for |
patient safety
|
| gptkbp:is_described_as |
guidance documents
|
| gptkbp:is_discussed_in |
industry conferences
technical journals |
| gptkbp:is_enhanced_by |
technological innovations
|
| gptkbp:is_essential_for |
clinical environments
|
| gptkbp:is_evaluated_by |
regulatory compliance
best practices independent laboratories |
| gptkbp:is_implemented_in |
healthcare facilities
|
| gptkbp:is_incorporated_in |
training programs
|
| gptkbp:is_influential_in |
medical device design
|
| gptkbp:is_informed_by |
field data
|
| gptkbp:is_integrated_with |
product lifecycle management.
other IEC standards |
| gptkbp:is_linked_to |
gptkb:ISO/_IEC_17025
|
| gptkbp:is_part_of |
quality management systems
medical device regulatory framework |
| gptkbp:is_promoted_by |
workshops
professional organizations |
| gptkbp:is_referenced_in |
gptkb:academic_research
gptkb:ISO_14971 |
| gptkbp:is_related_to |
gptkb:IEC_60601-1
|
| gptkbp:is_reviewed_by |
effectiveness
stakeholders |
| gptkbp:is_subject_to |
audits
|
| gptkbp:is_supported_by |
gptkb:software
gptkb:document |
| gptkbp:is_tested_for |
electromagnetic emissions
electromagnetic immunity |
| gptkbp:is_used_for |
compliance testing
|
| gptkbp:is_used_in |
healthcare industry
|
| gptkbp:is_utilized_in |
clinical trials
|
| gptkbp:part_of |
gptkb:IEC_60601_series
|
| gptkbp:provides_information_on |
risk management in EMC
|
| gptkbp:published_by |
gptkb:International_Electrotechnical_Commission
|
| gptkbp:regulatory_compliance |
regulatory bodies
|
| gptkbp:requires |
medical device manufacturers
|
| gptkbp:title |
Medical electrical equipment -Part 1-2: General requirements for basic safety and essential performance -Collateral standard: Electromagnetic compatibility -Requirements and tests
|
| gptkbp:updates |
to reflect technological advancements
|