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In the case of complaints related to this product, such
as damage to the knitted fabric or problems with
the fit, please contact the medical retailer directly.
Only serious incidents that may lead to a major
deterioration of the patient's medical condition or to
death should be reported to the manufacturer and
the relevant authority in the Member State. Serious
incidents are defined in Article 2 (65) Regulation (EU)
2017/745 (MDR).
Disposal
As a rule, the product is to be destroyed via the con-
ventional disposal route after the end of use. Please
observe the applicable local / national regulations.
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