3
EN
D-KAT Z-Type 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 Z-Type 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.
Summary of Contents for D-KAT Z
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