Keeler D-KAT R, Инструкция по эксплуатации

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EN
D-KAT Tonometer by KEELER
Consult instructions for use General warning sign
Date of manufacture Warning: Non-ionizing radiation
Manufacturer’s name and
address
Keep dry
Country of manufacture Fragile
Waste Electrical and Electronic
Equipment (WEEE) recycling
Do not use if package is
damaged
This way up Class II equipment
Temperature limit Atmospheric pressure limitation
Temperature limit Humidity limitation
0120
United Kingdom Conformity
Assessed, with the Notified
Body number for SGS UK
1639
Conformité Européene, with the
Notified Body number for SGS
Belgium NV
REP EC
Authorised representative in the
European Community
REP CH
Authorised representative in
Switzerland
Catalogue number Serial number
Translation Medical device
The Keeler D-KAT Tonometer is designed and built in conformity with Directive 93/42/EEC, Regulation (EU)
2017/745 and ISO 13485 Medical Devices Quality Management Systems.
Classification: CE / UKCA: Class IIa
FDA: Class II
The information contained within this manual must not be reproduced in whole or part without the manufacturer’s
prior written approval. As part of our policy for continued product development we the manufacturer reserve the right
to make changes to specifications and other information contained in this document without prior notice.
This IFU is also available on the Keeler UK and Keeler USA websites.
Copyright © Keeler Limited 2023. Published in the UK 2023.