Product Marking / Ce; Cleaning, Care And Disinfection; Technical Data - Petermann PM-5030 Gebrauchsanleitung

4 Product marking / CE

The Petermann Flexible Sliding Board is a Class I Medical Device and meets the EU-Regulation 2017/745 of
the European Parliament and Council dated 05.04.2017 for medical devices, also called MDR.
Petermann GmbH is certified in accordance with DIN EN ISO 13485 by TÜV Süd, Medical Devices - Quality
management systems applicable to the design and development, production and distribution of aids for
people of limited mobility.

5 Cleaning, care and disinfection

All Petermann repositioning and transfer aids can be wet cleaned. Use warm water and a mild cleaning agent. If
applicable, wipe the product off with a moist cloth and then let it dry thoroughly. Don't use any scouring or bleaching
agents or any sharp-edged objects for cleaning.
When necessary, we recommend wipe disinfection with the product Trionic
information upon request). As alternatives to our proven disinfectant Trionic
disinfectants for wipe disinfection:
Mikrobac Tissues*
®

Mikrobac forte*
®

Bacillol 30 Foam
®

Bacillol 30 Tissues
®

When using products marked with an *, wipe down again using a water-soaked cloth after disinfection has been
completed, in order to remove residues and prevent build-up. For wipe disinfection, please be sure to always follow
the instructions provided by the manufacturer.
Always follow the care instructions on the label of every product as well as the information in the respective user
manual.

6 Technical Data

Item no. Material
PM-5020 Polyethylene, latex free
PM-5030 Polyethylene, latex free
PM-5050 Polyethylene, latex free
, we can also recommend the following
®
Colour
black
black
black
16/33
(DGHM/VAH approval, further
®
Load-bearing capacity
200 kg
200 kg
200 kg