Liftup A/S | Hagensvej 21 | DK-9530 Støvring | Danmark | T: +45 96 86 30 20 | M: [email protected] | www.liftup.dk
USER MANUAL
–
RAIZER® M
–
GB VERSION 1.0
6
2.
EU declaration of conformity
Manufacturer:
Liftup A/SLiftup A/S
Address:
Hagensvej 21, DK-9530 Støvring
Phone:
+45 9686 3020
Reg. No.
523867 - Danish Medicines Agency
hereby declares that
Equipment:
RAIZER
®
M
Mobile lifting chair
The Raizer is in compliance with:
Medical Device Directive
MDD 93/42/EEC.
Medical devices under class 1 (according to rule
1 of annex IX of the Council Directive MDD 93/42/EEC). Conformity assessment was per-
formed according to Annex VII.
Raizer meets the relevant requirements notably in following standards:
EN/ISO 10535:2006
Hoists for the transfer of disabled persons
—
Requirements and
test methods
DS/EN 12182:2012
Assistive products for persons with disability - General require-
ments and test methods
The above product is manufactured under the following management system:
EN ISO 9001: 2015
Quality management, Certificate No. 5749-3027770-01-02-01
CEO
Søren Elisiussen
Position
Name
Liftup A/S, Hagensvej 21, DK-9530 Støvring, Denmark
Place
20 October 2020
Date
Signature
