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Liste Des Pièces De Rechange; Caractéristiques Techniques; Déclaration De Conformité - Dreve Injector control A Bedienungsanleitung

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Injector control A
Liste des pièces de rechange
1 Platine (électronique de commande)
2 Boîtier de chariot 2 pcs.
3 Entraînement de bande
4 Cuvettes de poignée 2 pcs.
5 Chargeur 220–230 V / 50–60 Hz
6 Chargeur 115 V / 60 Hz
7 Accu NiMH
Caractéristiques techniques
H x l x p
Poids
Tension secteur
Moteur CC
Vitesse de sortie d'engrenage min.
Vitesse de sortie d'engrenage max.
22
52438
52441
52443
52439ROT
1449LD
1449LUSA
52433
200 x 220 x 65 mm
env. 620 g avec accu intégré
220–230 V / 50–60 Hz, 115 V / 60 Hz
(tension/fréquence, voir plaque signalétique)
4 Watt / 12 V
0,35 1 / min – marche à vide
3,50 1 / min – marche à vide
Déclaration de conformité
According to EMV Directive (2014 / 30 / EU)
Herewith we declare that the machine described below in its conception and design and in the shape delivered
by us is in accordance with the fundamental safety and machine guidelines as prescribed in the applicable EC
directives.
In the case of any change or modification of the machine, not authorised by us, this declaration becomes invalid.
Denomination of the machine Injector control A
15151, 15151A
Type of machine
electromotive handheld device for double cartridges
Applicable EC directives
2014 / 30 / EU
EMV-Directive
Applied harmonised standards
2014 / 30 / EU
EMV-Directive
EN 61000-3-2:2014
Electromagnetic compatibility (EMC) – Part 3-2: Limits – Limits for har-
monic current emissions (equipment input current <= 16 Aper phase)
(IEC 61000-3-2:2014); German version EN 61000-3-2:2014.
EN 61000-3-3:2013
Electromagnetic compatibility (EMC) – Part 3-3: Limits – Limitation of volt-
age changes, voltage fluctuations and flicker in public low-voltage supply
systems, for equipment with rated current <= 16 Aperphase and not subject
to conditional connection (IEC 61000-3-3:2013); German version EN 61000-
3-3:2013.
EN 60601-1-2:2007 Ber1:2010-05 Medical electrical equipment – Part 1-2: General requirements for basic
safety and essential performance – Collateral standard: Electromagnetic
disturbances – Requirements and tests (IEC 62A/746/CD:2011) Medical
electrical equipment – Part 1-2: General requirements for basic safety
and essential performance – Collateral standard: Electromagnetic
compatibility – Requirements and tests (IEC 60601-1-2:2007, modified);
German version EN 60601-1-2:2007, Corrigendum to DIN EN 60601-
1-2 (VDE 0750-1-2):2007-12; German version CENELEC-Cor.: 2010 to EN
60601-1-2:2007.
Transient emission
EN 60601-1-2:2007 Ber1:2010-05 "General requirements for basic safety and essential performance" Prod-
uct standard for non life-sustaining devices, not operating, measuring or
monitoring of physical parameters.
Immunity
EN 60601-1-2:2007 Ber1:2010-05 "General requirements for basic safety and essential performance" Prod-
uct standard for non life-sustaining devices, not operating, measuring or
monitoring of physical parameters.
Dreve Otoplastik GmbH
Max-Planck-Str. 31
59423 Unna/Germany
www.dreve.com
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