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 1306, Item 1304, Item 1305, Item 1316, Item 1314, Item 1315	SEGUFIX®-Patent Twist Lock green
Item 1307, Item 1317	SEGUFIX®-Patent Twist Key yellow

according to the 2025 price list.

Basis-UDI-DI = PP01531120629 / Risk class = I

Intended use:

- Item 1306: closing of SEGUFIX® systems (for products manufactured after April 2003)
- Item 1307: quick release of the SEGUFIX®-Twist Lock green

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 -