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 5218, Item 5318, Item 5418, Item 5118

SEGUFIX®-Restraining Aid

according to the 2025 price list.

Basis-UDI-DI = PP01531521818 / Risk class = I

Intended use:

- provides assistance while restraining patients on stretchers
- after the restraint is applied, the SEGUFIX®-Restraining Aid may be removed
- additional stabilization of the patient
- can also be fastened above the knees
- also compatible for ambulance services
- Item 5218, Item 5318, Item 5418 – with locking system : physically restraining patients

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

R. W. de Sánchez

- Managing Director -