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Contents
Title
Page
Product Overview --------------------------------------------- 3
General Warnings ------------------------------- 4
Means of Delivery ---------------------------------- 5
Safety Instructions ---------------------------------- 5
Use Environments ---------------------------------- 6
Intended Use ----------------------------------------- 6
Technical Specification ---------------------------- 7
Accessories ------------------------------------------ 8
Electrical Specification----------------------------- 8
Assembly --------------------------------------------- 9
Assembly of Side Panels (optional) ---------- 11
Bed Controls and Indicators -------------------- 14
Floor-level Function ------------------------------ 16
Length Adjustment ------------------------------- 17
Functionality Check ------------------------------ 18
Using the Castor Brakes ------------------------ 18
Mattress Selection -------------------------------- 19
Siderail Selection --------------------------------- 20
Moving and Repositioning ---------------------- 20
Cable Routing for Mattress Pump ------------ 21
Cleaning & Disinfection-------------------------- 22
Troubleshooting ----------------------------------- 23
Storage ---------------------------------------------- 24
Daily Inspection ----------------------------------- 24
General Maintenance ---------------------------- 25
Guarantee ------------------------------------------ 25
Disposal --------------------------------------------- 25
EMC Statement ----------------------------------- 26
Table of Symbols --------------------------------- 30
Contact Details ------------------------------------ 31
Welcome
Dear Customer,
Thank you for purchasing an Accora
healthcare product. Before operating the
bed, you must read and understand all the
instructions in this manual. All actions and
handling of the bed must be performed in
accordance with the instructions in this
manual.
Please ensure that the manual is available to
users and operators throughout the bed’s
service life.
If you need further information, please
contact us. See section 28 for region specific
contact details.
General
The Empresa is classified as a Class 1
Medical Device in accordance with the
Medical Device Regulation 2017/745.
Notice to User
If a serious incident occurs in relation to this
medical device, affecting the user or the
patient, then the user or patient should report
the serious incident to the medical device
manufacturer (or distributor) and, in the
European Union, the user should also report
the serious incident to the Competent
Authority in the member state where they are
located.
Accora Ltd, 38 Main Street,
Swords, Co. Dublin, Ireland, K67 E0A2
T: +353 (0)1 695 0614
Design Policy and Copyright
® a
nd ™ are trademarks belonging to Accora Ltd
unless otherwise stated. As our policy is one of
continuous improvement, we reserve the right to
modify designs without prior notice. © Accora Ltd
2020.