Keeler Pulsair IntelliPuff, Instructions For Use Manual, Page: 6 / 110

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EN
Pulsair Intellipuff Tonometer by KEELER
Consult instructions for use General warning sign
Date of manufacture Warning: Non-ionizing radiation
Manufacturer’s name and
address
Warning: Electricity
Country of manufacture Warning: Optical radiation
Waste Electrical and Electronic
Equipment (WEEE) recycling
Warning: Floor level obstacle
This way up Keep dry
Type BF applied part Fragile
Temperature limit
Do not use if package is
damaged
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 Class II equipment
Serial number Atmospheric pressure limitation
Medical device Humidity limitation
Translation
The Keeler Pulsair Intellipuff 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.