NBN EN 61010-2-101 : 2003
Current
The latest, up-to-date edition.
SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT CONTROL AND LABORATORY USE - PART 2-101: PARTICULAR REQUIREMENTS FOR IN VITRO DIAGNOSTIC (IVD) MEDICAL EQUIPMENT
12-01-2013
1 Scope and object
2 Normative references
3 Terms and definitions
4 Tests
5 MARKING and documentation
6 Protection against electric shock
7 Protection against mechanical HAZARDS
8 Mechanical resistance to shock and impact
9 Protection against the spread of fire
10 Equipment temperature limits and resistance
to heat
11 Protection against HAZARDS from fluids
12 Protection against radiation, including laser
sources, and against sonic and ultrasonic
pressure
13 Protection against liberated gases, explosion
and implosion
14 Components
15 Protection by interlocks
16 Measuring circuits
Annex H Index of defined terms
Annex AA (normative) Risk management
Annex BB (informative) Instructions for use for self-test
IVD medical equipment
Annex ZA (normative) Normative references to international
publications with their corresponding European
publications
Bibliography
Applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.
| DocumentType |
Standard
|
| PublisherName |
Belgian Standards
|
| Status |
Current
|
| Standards | Relationship |
| I.S. EN 61010-2-101:2017 | Identical |
| DIN EN 61010-2-101 : 2017 | Identical |
| EN 61010-2-101:2017 | Identical |
| UNE-EN 61010-2-101:2004 | Identical |
| BS EN 61010-2-101:2017 | Identical |
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