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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 6710 SEGUFIX®-Transport Waist Belt Velcro
in the sizes offered according to the 2025 price list.
Basis-UDI-DI = PP01531621636 / Risk class = I

Intended use:

  • - to support patients in wheelchairs with a solid backrest, automobiles and other compatible seats
  • - not a restraint (note: some jurisdictions consider Velcro products as a restraint, should the patient not be able to remove them without help) Requirements:
  • - SEGUFIX®-Backrest Strap (item 6730) required
  • - SEGUFIX®-Suspender Belt (item 6720) if needed
  • - for a secure hold, the Velcro fastener must overlap at least 250 mm / 9.8 inches

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 -