Tabla De Contenido - Storz AUTOCON III 400 Manual De Instrucciones

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III
Inhalt
1
KARL STORZ Geräten ................................1
1. 1
Revisions-Index .......................................1
1. 2
Gültigkeit .................................................1
1. 3
Mitgeltende Dokumente ...........................1
1. 4
1. 4. 1
Aufbau von Warnhinweisen ....................2
1. 4. 2
1. 4. 3
Tipps ......................................................2
1. 4. 4
Kennzeichnungen ...................................3
2
Sicherheit .....................................................4
2. 1
2. 1. 1
Patientenprofil .........................................4
2. 2
Kontraindikationen ...................................4
2. 3
2. 4
2. 4. 1
Umgebungsbedingungen .......................6
2. 4. 2
2. 4. 3
Patienten ................................................7
2. 4. 4
2. 4. 5
2. 4. 6
Verwendung des Zubehörs .....................9
2. 5
Sicherheitshinweise ...............................10
2. 6
2. 6. 1
Explosionen/Zündung ...........................12
2. 6. 2
3
Beschreibung ............................................16
3. 1
Anzeige- und Bedienelemente ...............16
3. 1. 1
3. 1. 2
3. 1. 3
3. 1. 4
3. 2
Symbole am Produkt .............................19
3. 2. 1
Typenschild ..........................................21
3. 2. 2
Symbole auf Verpackung ......................21
3. 3
Lieferumfang ..........................................21
3. 4
Komponenten ........................................21
3. 5
Betriebsbedingungen .............................21
Contents
1
KARL STORZ devices .................................1
1. 1
Revision index..........................................1
1. 2
Validity .....................................................1
1. 3
Other applicable documents ....................1
1. 4
Symbols and labeling ...............................2
1. 4. 1
Structure of warnings .............................2
1. 4. 2
Risk levels in warnings ............................2
1. 4. 3
Tips ........................................................2
1. 4. 4
Other symbols and labeling ....................3
2
Safety ...........................................................4
2. 1
Intended use ............................................4
2. 1. 1
Patient profile .........................................4
2. 2
Contraindications .....................................4
2. 3
General safety information .......................5
2. 4
Personal safety instructions .....................6
2. 4. 1
Ambient conditions .................................6
2. 4. 2
Patients with pacemakers ......................6
2. 4. 3
2. 4. 4
2. 4. 5
Correct use of the HF device ..................8
2. 4. 6
and using accessories ............................9
2. 5
instructions ............................................10
2. 6
(general instructions) ..............................11
2. 6. 1
and explosions .....................................12
2. 6. 2
3
Description ................................................16
3. 1
Display and control elements .................16
3. 1. 1
3. 1. 2
3. 1. 3
3. 1. 4
3. 2
Symbols used on the device ..................19
3. 2. 1
Type plate .............................................21
3. 2. 2
Symbols on the packaging ...................21
3. 3
Scope of supply ....................................21
3. 4
operation ...............................................21
3. 5
Operating conditions..............................21
Contenido
1
1. 1
Índice de revisiones .................................1
1. 2
Validez .....................................................1
1. 3
1. 4
Símbolos e identificaciones ......................2
1. 4. 1
de advertencia .......................................2
1. 4. 2
indicaciones de advertencia ...................2
1. 4. 3
Sugerencias ...........................................2
1. 4. 4
2
Seguridad .....................................................4
2. 1
Uso previsto ............................................4
2. 1. 1
Perfil del paciente ...................................4
2. 2
Contraindicaciones ..................................4
2. 3
2. 4
2. 4. 1
Condiciones ambientales ........................6
2. 4. 2
Pacientes con marcapasos ....................6
2. 4. 3
2. 4. 4
2. 4. 5
2. 4. 6
empleo de los accesorios .......................9
2. 5
específicas del producto ........................10
2. 6
2. 6. 1
explosiones/inflamación ........................12
2. 6. 2
3
Descripción ................................................16
3. 1
3. 1. 1
delantera ..............................................16
Módulo de conector unipolar (izquierda) .17
3. 1. 2
3. 1. 3
Módulo de conexión bipolar (derecha) ..17
3. 1. 4
trasera ..................................................18
3. 2
3. 2. 1
Placa de especificaciones ....................21
3. 2. 2
3. 3
Volumen de suministro ...........................21
3. 4
para el funcionamiento ..........................21
3. 5
Condiciones de servicio .........................21

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