Stryker SmartPump Instrucciones De Uso página 61

DE
Technische Daten (Fortsetzung)
Zeitanzeige:
Druckanzeige:
Schutz gegen Eindringen (IP):
Geräteklassifikation und -typ:
Produktsicherheitszertifizierung:
28
Inflationsdauer numerisch
Bereich: 1 bis 240 Minuten
von 1 bis 15 Minuten in 1-Minuten-Stufen;
Regulierung:
von 15 bis 240 Minuten in 5-Minuten-Stufen
Ist-Wert digital numerisch mit Druckmessergrafik
Genauigkeit: ± 2% bzw. (falls größer) 4 mmHg Abweichung vom eingestellten
Druckwert
Bereich: 100 bis 475 mmHg
IPX0
International Electrotechnical Commission (IEC)
IEC 60601-1:1988, Medical Electrical Equipment — Part 1: General
Requirements for Safety - Second Edition; Amendment 1 (1991);
Amendment 2 (1995); Corrigendum 1 (1995)
Canadian Standards Association (CSA)
CAN/CSA-C22.2 No. 601.1-M90, Medical Electrical Equipment —
Part 1: General Requirements for Safety
Underwriters Laboratories (UL)
UL 60601-1, Medical Electrical Equipment, Part 1: General
Requirements for Safety — First Edition; Revisions through and
including April 26, 2006
International Electrotechnical Commission (IEC)
IEC 60601-1:2005, Ed:3, Medical Electrical Equipment — Part 1:
General Requirements for Basic Safety and Essential Performance;
Corrigendum 1 (2006); Corrigendum 2 (2007)
Canadian Standards Association (CSA)
CAN/CSA-C22.2 No. 60601-1:08, Medical Electrical Equipment —
Part 1: General Requirements for Basic Safety and Essential
Performance
American National Standards Institute (ANSI)/Association for the
Advancement of Medical Instrumentation (AAMI)
ANSI/AAMI ES60601-1:2005, Medical Electrical Equipment — Part 1:
General Requirements for Basic Safety and Essential Performance;
Consolidated Reprint (2009); Amendment 2 (2010)
European Committee for Electrotechnical Standardization (CENELEC)
EN 60601-1:2006, Ed:3, Medical Electrical Equipment – Part 1:
General Requirements for Basic Safety and Essential Performance;
IEC Corrigendum 1 (2006); IEC Corrigendum 2 (2007); CENELEC
Corrigendum (2010); CENELEC Amendment A11 (2011)
Elektrisches Medizinprodukt der Klasse I,
defibrillationssicher, Teil mit Patientenkontakt vom Typ BF
CSA International
5920-011-712 Rev-H
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