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4.4
Labels
Text/symbol
Name and address of manufacturer, date of manufacture
Unique Device Identification
UDI
(product identification number as per Directive (EU) 2017/745)
Article number
Serial number
ProdID
seca product identification number
Follow instructions for use
Medical electrical device, Type B
Value in units of mass (non-verified models)
d
States the difference between two consecutive display values
Type of protection to IEC 60529:
• Protection against ingress of solid foreign bodies with a diameter of over 12.5 mm
IP20
• Protection against access with fingers
• No protection from ingress of water
Device complies with EU directives
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
xxxx
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
Markings on the device and on the type plate
: Notified Body for Medical Devices of the United Kingdom
Meaning
English
Overview • 13
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