NS EN ISO 17510-1 : 2009
Current
The latest, up-to-date edition.
SLEEP APNOEA BREATHING THERAPY - PART 1: SLEEP APNOEA BREATHING THERAPY EQUIPMENT
12-01-2013
Foreword
Introduction
Section one - General
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements and general requirements
for test
5 Classification
6 Identification, marking and documents
7 Power input
Section two - Environmental conditions
8 Basic safety categories
9 Removable protective means
10 Environmental conditions
11 Not used
12 Not used
Section three - Protection against electric shock hazards
13 General
14 Requirements related to classification
15 Limitation of voltage and/or energy
16 Enclosures and protective covers
17 Separation
18 Protective earthing, functional earthing
and potential equalization
19 Continuous leakage currents and patient
auxiliary currents
20 Dielectric strength
Section four - Protection against mechanical hazards
21 Mechanical strength
22 Moving parts
23 Surfaces, corners and edges
24 Stability in normal use
25 Expelled parts
26 Vibration and noise
27 Pneumatic and hydraulic power
28 Suspended masses
Section five - Protection against hazards from unwanted
or excessive radiation
29 X-radiation
30 Alpha, beta, gamma, neutron radiation and other
particle radiation
31 Microwave radiation
32 Light radiation (including lasers)
33 Infra-red radiation
34 Ultra-violet radiation
35 Acoustical energy (including ultra-sonics)
36 Electromagnetic compatibility
Section six - Protection against hazards of ignition of
flammable anaesthetic mixtures
37 Locations and basic requirements
38 Marking, accompanying documents
39 Common requirements for Category AP and category
APG equipment
40 Requirements and tests for category AP equipment,
parts and components thereof
41 Requirements and tests for category APG equipment,
parts and components thereof
Section seven - Protection against excessive temperatures and other
safety hazards
42 Excessive temperatures
43 Fire prevention
44 Overflow, spillage, leakage, humidity, ingress
of liquids, cleaning, sterilization and disinfections
45 Pressure vessels and parts subject to pressure
46 Not used
47 Electrostatic charges
48 Biocompatibility
49 Interruption of the power supply
Section eight - Accuracy of operating data and protection
against hazardous output
50 Accuracy of operating data
51 Protection against hazardous output
Section nine - Abnormal operation and fault conditions;
environmental tests
52 Abnormal operation and fault conditions
53 Environmental tests
Section ten - Constructional requirements
54 General
55 Enclosures and covers
56 Components and general assembly
57 Main parts, components and layout
58 Protective earthing - terminals and connections
59 Construction and layout
Annexes
Annex AA (informative) Rationale
Annex BB (informative) Glossary
Annex ZA (informative) Clauses of this European standard
addressing essential requirements or other
provisions of EU directives
Annex ZB (normative) Normative references to international
publications with their relevant European
publications
Bibliography
Describes requirements for equipment intended for sleep apnoea breathing therapy for domiciliary use, ships, aircraft and other transport vehicles and for use in healthcare institutions.
DocumentType |
Standard
|
PublisherName |
Norwegian Standards (Norges Standardiseringsforbund)
|
Status |
Current
|
Standards | Relationship |
ONORM EN ISO 17510-1 : 2009 | Identical |
SN EN ISO 17510-1 : 2009 | Identical |
UNI EN ISO 17510-1 : 2009 | Identical |
ISO 17510-1:2007 | Identical |
NF EN ISO 17510-1 : 2009 | Identical |
UNE-EN ISO 17510-1:2009 | Identical |
BS EN ISO 17510-1:2009 | Identical |
I.S. EN ISO 17510-1:2009 | Identical |
EN ISO 17510-1:2009 | Identical |
DIN EN ISO 17510-1:2009-07 | Identical |
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