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SEGUFIX
CE

EU Declaration of Conformity

In accordance with Art. 52 No. 7 of the EU Regulation EU 2017/745 of the Council on Medical Devices (of 05.04.2017) declares

SEGUFIX®-Bandagen, Das Humane System GmbH & Co. KG (SRN: DE-MF-000027702), hereby declares under sole responsibility that the basic safety and performance requirements according to Annex I of this regulation are met for the following medical device:

Item 5243, Item 5343, Item 5443, Item 5143 SEGUFIX®-Stretcher Restraint Shoulder
in the sizes offered according to the 2025 price list.
Basis-UDI-DI = PP01531524335 / Risk class = I

Intended use:

  • - to secure patients on stretchers
  • - also compatible with ambulance stretchers
  • - physically restraining patients Requirements: SEGUFIX®-Hand Restraint extended and SEGUFIX®-Stretcher Restraint Foot required

The conformity assessment procedure according to Annexes II and III of the EU Regulation EU 2017/745 has been applied. This declaration is valid from the date of issue until May 24th, 2028.

Jesteburg, May 25th, 2026
Date of issue
Signature
R. W. de Sánchez
- Managing Director -