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6.2.
Normes
Normes référencées par Directive 93/42/EEC
Standard
EN60601-1: 1990
EN60601-1/A1: 1993
EN60601-1/A2: 1995
EN60601-1/A13:
1996
EN60601-1-1: 2001
EN60601-1-2: 2001
EN60601-1-4: 1996
EN60601-1-4/A1:
1999
EN 60601-2-30
Normes référencées par Directive 1999/5/EC
Standard
ETSI EN 301 489-17
v 1.2.1 (2002-08)
ETSI EN 300 328
v 1.7.1 (2006-10)
Notice d'emploi: um_walk200b_cardiolinespa_05_fra01.doc
Via De Zinis, 6
Cardioline S.p.A.
Via F.lli Bronzetti, 8
Sales office:
Titre
Medical electrical equipment - Part 1: General requirements
for safety
Medical electrical equipment - Part 1-1: General requirements
for safety – Collateral standard: Safety requirements for
medical electrical systems
Medical electrical equipment - Part 1-2: General requirements
for safety – Collateral standard: Electromagnetic compatibility
- Requirements and tests
Medical electrical equipment - Part 1-4: General requirements
for safety – Collateral standard:
medical systems
Medical
electrical
requirements for the safety, including essential performance,
of automatic cycling non-invasive blood pressure monitoring
equipment
Titre
Electromagnetic compatibility and Radio spectrum Matters
(ERM); Electromagnetic Compatibility (EMC) standard for
radio equipment and services;
Part
17:
Specific
transmission systems and 5 GHz high performance RLAN
equipment
Electromagnetic compatibility and Radio spectrum Matters
(ERM); Wideband transmission systems; Data transmission
equipment operating in the 2,4 GHz ISM band and using
wide band modulation techniques; Harmonized EN covering
essential requirements under article 3.2 of the R&TTE
Directive.
38011 Cavareno (TN) Italy
20129 Milano (MI) Italy
walk200b
Programmable electrical
equipment
-
Part
conditions
for
2,4
info@cardioline.it
tel.+39 02 94750470
2-30:
Particular
GHz
wideband
31/40
www.cardioline.it
fax +39 02 94750471
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