Safety
4990851_002_00 – 2082262 – 2022-01-10 13
1.7 Disposal
Within the European Union the product is governed by Directive
2012/19/EU on waste electrical and electronic equipment and
complies with the requirements of Directive 2011/65/EU of the
European Parliament and of the Council of 8 June 2011 on the
restriction of the use of certain hazardous substances in electrical
and electronic equipment as amended by Commission Delegated
Directive (EU) 2015/863 of 31 March 2015 as regards the list of
restricted substances (RoHS). The operating table must not be
disposed of via public collection points for waste electronic
devices.
In countries outside the European Union (EU), the legal
requirements of the respective country must be observed.
Please contact the Trumpf Medizin Systeme Technical Customer
Service, the local sales representative or the appropriate national
authority if you have any questions about proper disposal.
In addition to regional disposal, faulty products or products that
are no longer used may be returned to Trumpf Medizin Systeme.
Trumpf Medizin Systeme then takes responsibility for
environmentally friendly disposal. Detailed information on returns
is available from the Trumpf Medizin Systeme Technical Customer
Service.
If the operating table is decommissioned, the lead–acid battery
must be removed from the operating table by a qualified service
technician. Once removed, the batteries must be sent to the
Trumpf Medizin Systeme Technical Customer Service, using
suitable packaging. Attention: when returning batteries, the
package must be declared as containing hazardous materials of
Class 8/UN2794.
1.8 Test procedures
As the medical products from Trumpf Medizin Systeme are
distributed worldwide, uniform guidelines for electrical retesting
should be used.
According to the IEC 62353 standard, the limit values according to
the CF classification apply when testing applied parts. Due to its
design, the Trumpf Medizin Systeme PST 300 operating table
contains only one application part in Class B.
Furthermore, the Trumpf Medizin Systeme product-specific
prescribed retests and safety checks are obligatory.
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