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EN
Espire Elleboog Pro & Hybrid van Steeper Group, distributeur Loth Fabenim B.V.
Espire
TM
Elleboog Pro & Hybrid Instruction Manual - For Prosthetists
62
Intended Use and Safety
13
Complies with Standards
No.
Description
Version
ISO 22523
External limb prostheses and external
orthoses – Requirements and test
methods
2006
AAMI ANSI 60601-1
Medical Electrical Equipment – Part 1:
General requirements for basic safety
and essential performance
2007/ (R)
2012 and
A1:2012
IEC 60601-1-2
Medical Electrical Equipment – Part 1-2:
General requirements for basic safety
and essential performance – Collateral
standard: Electromagnetic compatibility
– Requirements and tests
Edition
4.0 2014
IEC 60601-1-6
Medical Electrical Equipment – Part 1-6:
General requirements for basic safety
and essential performance – Collateral
standard: Usability
2013 Ed 3.1
IEC 62366-1
Medical Devices – Part 1: Application of
Usability Engineering to Medical Devices
2015 Ed 1
IEC 60601-1-11
Medical Electrical Equipment – Part 1-11:
General requirements for basic safety
and essential performance – Collateral
standard: requirements for medical
electrical equipment and medical
electrical systems used in the home
healthcare environment
2015 Ed 2
IEC 62304
Medical Device Software – Software Life
Cycle Processes
2006 Ed 1 + A1
ISO 10993-1
Biological evaluation of medical devices
– Part 1: Evaluation and testing within a
risk management process
2009
ISO 10993-5
Biological evaluation of medical devices
– Part 5: Tests for in vitro cytotoxicity
2009
ISO 10993-10
Biological evaluation of medical devices
– Part 5: Tests for in vitro cytotoxicity
2010