Service Request; Life Span; Demolition; Reference Standards - Promeba PA210-O User Manual

USER GUIDE
SPINE BOARD
02 INTRODUCTION
02.3.

Service request

For information of the correct interpretation of the instruction manual, the use, maintenance,
installation and restoration of the product, please contact Promeba customer service: T. 93
837 12 00, email: promeba@promeba.com or write to PROMEBA, S.L. - Ctra C-16 Km 59.5
· 08650 Sallent (Barcelona) · SPAIN.
Whenever you want to communicate any matter related to a product, you will be asked for
the product reference (
the label containing this information and found on the original packaging of the product.
02.4.

Life span

If used as described in the following instructions, this device has a useful life of 10
years from the date of purchase.
This useful life can be extended with annual reviews carried out by the manufacturer, which
uses specialized and authorized internal and external technicians.
In case these annual checks are not carried out, the device must be disposed of according
to the information in paragraph 02.5 and the manufacturer must be notified.
Only the manufacturer or an authorized center can extend the life of the device, if it meets
the safety and legal requirements.
Promeba, S.L. will not accept any responsibility for malfunction or damage caused by the use
of devices that have not been checked by the manufacturer or authorized center, or that have
exceeded the maximum allowed useful life.
02.5.

Demolition

When the devices are no longer suitable for use, if they have not been contaminated by any
particular agent, they can be disposed of as normal solid waste, otherwise, follow the current
demolition regulations.
02.6.

Reference standards

REFERENCE
EU Regulation 2017/745
As a distributor or end user of the products manufactured and/or distributed by Promeba, S.L., you are
strictly obliged to know the legal provisions in force in the country of destination of the goods, applicable
to the devices to be supplied (including the regulations relating to technical specifications and/or safety
requirements) and, therefore, understand the necessary requirements to ensure compliance of the
products themselves with all the legal requirements of the territory.
REV. 2023/05
) and the serial number (
EU Regulation on Medical Devices
EN
). It is strongly recommended to keep
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