Spare Part List; Declaration Of Conformity; Technical Data - Dreve Injector control A Bedienungsanleitung

Injector control A

Spare part list

1 Circuit board (electronic control)
2 Housing of the piston guide 2 pcs.
3 Tape drive unit
4 Molded recess 2 pcs.
5 Charger 220–230 V / 50–60 Hz
6 Charger 115 V / 60 Hz
7 NiMH Accu

Technical Data

H x W x D
Weight
Voltage
DC motor
min. multistage speed
max. multistage speed
14
52438
52441
52443
52439ROT
1449LD
1449LUSA
52433
200 x 220 x 65 mm
approx. 620 g with integrated accu
220–230V / 50–60Hz, 115V / 60Hz
(Voltage / frequency see at type plate)
4Watt / 12V
0.35 r / min – idle speed
3.50 r / min – idle speed

Declaration of conformity

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
voltage changes, voltage fluctuations and flicker in public low-voltage sup-
ply 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
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www.dreve.com
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