Seca 675 Bedienungsanleitung Seite 42

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Device complies with EU directives
•
•
M24 0102
0123
•
•
Medical device in accordance with regulation (EU) 2017/745
MD
Device meets the requirements of the USA and Canada. Certified and tested by a licensing labo-
ratory (NRTL) of TÜV SÜD Product Services GmbH.
Device complies with United Kingdom directives
•
•
•
•
Importer/representative in the United Kingdom:
seca Ltd
40 Barn Street
B5 5QB Birmingham
UK REP United Kingdom
Importer/representative in Switzerland:
seca ag (schweiz)
Medizinische Waagen und Messsysteme
Schönmatt Str. 2
CH REP
CH-4153 REINACH
Type plate on the power supply connection socket
• Power supply voltage required in V
• Maximum current consumption in mA
x-y V
•
max. xxx mA
use compatible
•
seca adapter only
•
Do not dispose of device in household waste
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Protect from moisture
Arrows indicate top of product
Transport and store in an upright position
Fragile, do not throw or drop
42 • seca 675/seca 674
Markings on the device and on the type plate
: Conformity label in compliance with directive 2014/31/EU for non-automatic scales (verified
M
models)
: (Example: 2024) Year in which declaration of conformity was implemented and the CE-label
24
was applied (verified models)
: Notified Body for Metrology (verified models)
0102
: Notified Body for Medical Devices
0123
: Conformity label in compliance with UK directive SI 2016 no. 1152 for non-automatic scales
M
(NAWIR) (verified models)
24 : (Example: 2024) Year in which declaration of conformity was implemented and the UKCA la-
bel was applied (verified models)
xxxx : Notified Body for Medical Devices of the United Kingdom
: Notified Body for Metrology of the United Kingdom (verified models)
yyyy
: Note polarity of device connector
: Operate device with direct current
: Use compatible seca power supply units only
Markings on the packaging
Meaning
Meaning