Seca mBCA 555 Instrucciones De Uso página 121

Symbol
Device complies with EU directives
• : Conformity label in compliance with directive 2014/31/EU for non-automatic scales (verified
M
models)
0102 • : (Example: 2022) Year in which declaration of conformity was implemented and the CE label
M22 22
0123
was applied (verified models)
• : Notified Body for Metrology (verified models)
0102
• : Notified Body for Medical Devices
0123
MD
Medical device in accordance with Regulation (EU) 2017/745
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
• : Conformity label in compliance with UK directive SI 2016 no. 1152 for non-automatic scales
M
(NAWIR)(verified models)
• : (Example: 2022) Year in which declaration of conformity was implemented and the UKCA la-
22
bel was applied (verified models)
• : Notified Body for Medical Devices of the United Kingdom
xxxx
• : Notified Body for Metrology of the United Kingdom (verified models)
yyyy
Importer/representative in the United Kingdom:
seca Ltd
40 Barn Street
UK REP B5 5QB Birmingham
United Kingdom
Importer/representative in Switzerland:
seca ag (schweiz)
Medizinische Waagen und Messsysteme
CH REP Schönmatt Str. 4
CH-4153 REINACH
Symbol of the US Federal Communications Commission (FCC)
Device license number from the US Federal Communications Commission (FCC)
FCC ID
IC ID Device license number from Industry Canada
Markings on the device and on the type plate
Meaning
English
Overview • 121