Keeler Pulsair IntelliPuff Gebrauchsanleitung Seite 6

Pulsair Intellipuff Tonometer by KEELER
Consult instructions for use
Date of manufacture
Manufacturer's name and
address
Country of manufacture
Waste Electrical and Electronic
Equipment (WEEE) recycling
This way up
Type BF applied part
Temperature limit
United Kingdom Conformity
Assessed, with the Notified
0120
Body number for SGS UK
Authorised representative in the
EC REP
European Community
Catalogue number
Serial number
Medical device
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.
EN
General warning sign
Warning: Non-ionizing radiation
Warning: Electricity
Warning: Optical radiation
Warning: Floor level obstacle
Keep dry
Fragile
Do not use if package is
damaged
Conformité Européene, with the
Notified Body number for SGS
1639
Belgium NV
Authorised representative in
CH REP
Switzerland
Class II equipment
Atmospheric pressure limitation
Humidity limitation
2