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Klinische Genauigkeit: Entsprechend des AAMI-SP10 mit auskultatorischer
Referenz:
< 5 mmHg Systemabweichung
< 8 mmHg Standardabweichung
Aufpumpen: Automatisch
Entlüften: «Schrittweise»/Ablassventil
Batterien: 2 Batterien, Type LR 03 (AAA)
Betriebstemperatur: + 10 °C bis +40 °C
Aufbewahrungstemperatur: 20 °C bis +60 °C
Luftfeuchtigkeit: Bis zu 85% rel. Luftfeuchtigkeit
Manschette: Geeignet für Handgelenksumfang von 13 bis 21 cm
Klinische Validierung: Entsprechend AAMI-SP10 mit auskultatorischer
Referenz. (Wichtig: Validierung gegen intra-arterielle
Messungen kann zu abweichenden Ergebnissen führen
– für Geräte, die gegen auskultatorische Referenz
kalibriert sind.)
Beim Einsatz des Gerätes außerhalb der festgelegten Temperatur- und Feuchtig-
keitsbereiche kann die technische Genauigkeit nicht sichergestellt werden.
Anwendungsteil des Typs BF
Änderungen vorbehalten.
Dieses Gerät entspricht folgenden Normen:
DIN EN 60601-1: 3/96 «Medizinische elektrische Geräte» –
Teil 1: Allgemeine Festlegungen für die Sicherheit
DIN EN 1060-1: 12/95, AMD 1 09/02 «Nichtinvasive Blutdruck-Messgeräte» –
Teil 1: Allgemeine Anforderungen
DIN EN 1060-3: 9/97 «Nichtinvasive Blutdruck-Messgeräte» –
Teil 3: Ergänzende Anforderungen für elektromechanische Blutdruck-Messgeräte
Dieses Gerät entspricht den Bestimmungen der EG-Richtline 93/42/EEC
(Richtlinie für medizinische Geräte).
0297
6073426_BP1650_MN Seite 12 Montag, 4. Dezember 2006 9:20 09
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  • Le tensiomètre Braun Kronberg Type 6071 affiche t il un message en cas d'arythmie cardiaque Submitted on 26-7-2023 at 12:26

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  • Le tensiomètre Braun Kronberg type 6071 affiche-t-il un message particulier en cas d'arythmie cardiaque ? Submitted on 26-7-2023 at 12:23

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